Chemical and biological agents for the control of molluscs

ABSTRACT

Compositions and methods for controlling molluscs, members of the Gastropoda and Bivalvia classes which includes but is not limited to lactones, lactams, carbamates, amides, and/or carboxylic acid containing compounds as active ingredients and/or compounds derived from  Pseudomonas  and/or  Erwinia . Also provided are methods and compositions for increasing the efficacy of chemical and biological control for invasive molluscs in open waters, power plants, and drinking water treatment facilities under coldwater conditions.

PRIORITY CLAIM

This application claims priority from U.S. application Ser. No.61/170,686, filed Apr. 20, 2009, U.S. application Ser. No. 61/170,790,filed Apr. 20, 2009 and U.S. application Ser. No. 61/170,790, filed Dec.10, 2010, the contents of which are incorporated herein by reference.

FIELD OF THE INVENTION

Compositions and methods for controlling molluscs, such as musselsand/or snails and/or slugs which includes but is not limited tolactones, lactams, carbamates, amides, and/or carboxylic acid containingcompounds as active ingredients and/or compounds derived from a microbe(e.g., Pseudomonas and/or Erwinia). Also provided are methods andcompositions for increasing the efficacy of chemical and biologicalcontrol for molluscs, such as mussels and/or snails and/or slugs in openwaters, power plants, and drinking water treatment facilities undercoldwater conditions or solid surfaces.

BACKGROUND OF THE INVENTION

The Zebra mussel, Dreissena polymorpha, was originally native to theCaspian Sea and the Ural River in Asia. In the nineteenth century, itspread west and now occurs in most of Europe, the western portion of theCommonwealth of Independent States (formally the Soviet Union), andTurkey. Over two decades ago, the mussels, such as zebra mussel,Dreissena polymorpha and quagga mussel, Dreissena bugensis, wereintroduced into North America. Their wide spread through inland watershas led to the coverage of most of eastern of US [U.S. Army EngineerWaterways Experiment Station. 1995. Zebra mussels: Biology, Ecology, andRecommended Control Strategies. Technical Note. ZMR-1-01. Zebra MusselResearch Program, Vicksburg, Miss.]. Similarly, Golden Mussel,Limnoperna fortune, affected Asian and Southern American countries(Golden Mussel—Limnoperna fortune). Asian Clam Corbicula fluminea almostspread all Asian countries and US [Non-indigenous species informationbulletin: Asian clam, Corbicula fluminea (Müller, 1774) (Mollusca:Corbiculidae)]. And other mussels such unionid mussels exist in US andother countries.

The ability of the mussels to quickly colonize new areas, rapidlyachieve high densities and attach to any hard substratum (e.g., rocks,logs, aquatic plants, shells of native mussels, and exoskeletons ofcrayfish, plastic, concrete, wood, fiberglass, pipes made of iron andpolyvinyl chloride and surfaces covered with conventional paints) makethem to cause serious adverse consequences. These consequences includedamages of water-dependent infrastructure, increased millions of dollarsin the operating expense and significant damage of the ecologicalsystems [O'Neill, C. R., Jr. 1997, Economic impact of zebramussels-results of the 1995 national zebra mussel information clearinghouse study. Gt. Lakes Res. Rev. 3, 35-44; Karatayev, A. Y., L. E.Burlakova, D. K., Padilla, 1997, the effects of Dreissena polymorpha(Pallas) invasion on aquatic communalities in eastern Europe. JournalShellfish Research, 16, 187-203; MacIsaac, H. J., 1996. Potentialabiotic and biotic impacts of zebra mussels on the inland waters ofNorth America. American Zoology, 36, 289-299; D. P. Molloy, thepotential for using biological control technologies in the management ofDreissena SPP, Journal of Shellfish Research, 1998 (17) 177-183] as wellas productivity reduction which costs billions of dollars in lostrevenue (Connelly, N. A., C. R. O'Neill, Jr, et al. (2007), “Economicimpacts of Zebra mussels on drinking water treatment and electric powergeneration facilities”, Environmental Management 90:10. Economic impactsof zebra mussels on drinking water treatment and electric powergeneration facilities. Environmental Management 40: 105-112).Additionally, rapid invasion of aquatic ecosystems by these invasivemussels has caused decline in the richness and abundance of endemicunionid mussels, an important part of biodiversity (Ricciardi, A, Neves,R. J., Rasmussen, J. B. 1998. Impending extinctions of North Americanfreshwater mussels (Unionidae) following the zebra mussel (Dreissenapolymorpha) invasion. Journal of Animal Ecology 67: 613-619).

Management of mussels is very important for protecting water-dependentinfrastructure and water ecological systems. There are many ways toreduce the populations of mussels. These methods include pre-active andreactive methods. Reactive removal includes the mechanical removal,predator removal, and chemical and biochemical removal. For example,fish, birds, crayfish, crabs, leeches and mammals have shown to predatemussels. However, it is unlikely that mussel population will becontrolled by natural predation, especially in man-made structures suchas pipes or pumping plants.

Application of molluscicides is another effective ways to reduce themussel population. For example, sodium hypochlorite is a commonly usedcontrol agent in Europe, US, and Canada. However, mussels can withstandthis treatment for several days by closing their shells and chlorine canbe only used in pipes or ducts that contain pressure sensing or otherequipment due to environmental toxicity of chlorine [U.S. Army EngineerWaterways Experiment Station. 1995. Zebra mussels: Biology, Ecology, andRecommended Control Strategies. Technical Note. ZMR-1-01. Zebra MusselResearch Program, Vicksburg, Miss.]. In addition, there are many othercommercialized molluscicides such as surfactant ammonium salts,Butylated hydroxytoluene (BHT) in paints, N-triphenylmethyl-morpholineand so on. These chemicals either low selectivity or affect the waterecosystems. For example, a 4-trifluoroethyl-4-nitrophenol marketed asBayluscide® (Bayer) is a possible candidate for control such invasiveexotic species. However, the toxic mechanism of such a chemical is toaffect mussel cellular respiration, which in nature will limit itsselectivity between mussel and other aquatic species such as fish [KarenPerry

John Lynn, Detecting physiological and pesticide-induced apoptosis inearly developmental stages of invasive bivalves, Hydrobiologia (2009)628:153-164; I Takougang, J Meli, F Angwafo, Field trials of low doseBayluscide on snail hosts of schistosome and selected non-targetorganisms in sahelian Cameroon, Mem Inst Oswaldo Cruz, Rio de Janeiro,2006, 101(4): 355-358].

It is crucial to manage the invasive mussels in a safe, environmentalfriendly and cheap manner. In order to find less harmful methods tocontrol these invasive mussels, New York State Museum's (NYSM) FieldResearch Laboratory screened more than 700 bacterial isolates aspotential biological control agents to be used against zebra and quaggamussels. As a result, they found an isolate, strain CL145A ofPseudomonas fluorescens, to be lethal to these mussels (see Molloy, D.P. U.S. Pat. No. 6,194,194, issued Feb. 27, 2001). This bacterium isworldwide in distribution and is present in all North Americanwaterbodies. In nature it is a harmless bacterial species that is foundprotecting the roots of plants from rot and mildew. It is so ubiquitousthat it is a common food spoilage organism in the average householdrefrigerator [Daniel P. Molloy and Denise A. Mayer, Overview of a NovelGreen Technology: Biological Control of Zebra and Quagga Mussels withPseudomonas fluorescens, Version 6: Updated Aug. 24, 2007].

Lactones, Lactams, Carbamate and Amides

Lactones are widely distributed in foods and beverages, and are alsosecondary metabolites of animals (e.g., sponges) and microorganisms(e.g., yeasts, fungi). Some lactones have a special aroma (e.g.,gamma-decalactone), resulting in an increasing demand for naturalproducts in food industry by the use of biotechnological processes forthe production of these lactones [Mohamed Alchihab, Jacqueline Destain,Mario Aguedo, Lamia Majad, Hakim Ghalfi, Jean-Paul Wathelet, PhilippeThonart, Production of γ-Decalactone by a Psychrophilic and a MesophilicStrain of the Yeast Rhodotorula aurantiaca, Appl Biochem Biotechnol(2009) 158:41-50]. Other functions of different lactones are associatedwith antibacterial activity [Ikuko Shimizu, Yasunori Isshiki, HarueNomura, Keisuke Sakuda, Katsuya Sakuma, Seiichi Kondo, The AntibacterialActivity of Fragrance Ingredients against Legionella pneumophila, Biol.Pharm. Bull. 2009, 32(6) 1114-1117], hepatoprotective activity [YumikoItoh, Hiroshi Shimura, Mayumi Ito, Naoharu Watanabe, Michio Yamagishi,Masaharu Tamai and Kazunori Hanada, Novel hepatoprotective γ-lactone,MH-031, I. Discovery isolation, physicochemical properties andstructural elucidation, The Journal of Antibiotics 1991, 832-837],anti-tuberculosis activity [Ma, G. Y. et al. anti-tuberculosisconstituents from the stem bark of micromelum hirsutum, Planta Med.2005, 71, 261-267], anti-HIV activity [zhang et al., sesquiterpenes andbutenolides, natural anti-HIV constituents from Litse verticillata,Planta Med, 2005, 71, 452-457], sex pheromone [J. H. Tumlinson,Identification of the Female Japanese Beetle Sex Pheromone Inhibition ofMale Response by an Enantiomer, Science, 1977, 197, 789-792], cytotoxicactivity [Fan, X. N. et al. Chemical Constituents of Heteroplexismicocephala, J. Nat. Prod. 2009, 72, 1184-1190], signal molecules [M. K.Vinson, et al. Multiple N-acyl-L-homoserine lactone signal moleculesregulate production of virulence determinants and secondary metabolitesin Pseudomonas aeruginosa, Proc. Natl. Acad. Sci. USA, 1995, 92,9427-9431] and insecticidal activity [John A. Findlay, et al., Insecttoxins from spruce endophytes, Can. J. Chem. 2003, 81, 284-292],

Although lactams exist in some plants and marine organisms, they oftenare fungal metabolites. Many biological activities (e.g., cytotoxic andantitumor activity, angiogenesis inhibition, neuronal activity,anti-infectious activities) were reviewed in a recent publication[Bastien Nay, Nassima Riache and Laurent Evanno, Chemistry and biologyof non-tetramic γ-hydroxy-γ-lactams and γ-alkylidene-γ-lactams fromnatural sources, Natural Product reports, 2009, 26, 1044-1062].

Carbamates exist in plants, microorganism and sponges, but fewerbiological activities are reported for these compounds in comparisonwith lactones, amides because many of these compounds are not stable inaqueous solutions. There was one example of fungicidal activity ofnatural carbamates [Richard J. Clark, et al., Antifungal Alkyl AminoAlcohols from the Tropical Marine Sponge Haliclona n. sp., J. Nat. Prod.2001, 64, 1568-1571]. 1. Amides are widely distributed in plants,microorganisms and sponges. For example, Scalusamide A frommarine-derived fungus Penicillium citrinum exhibited antibacterial andantifungal activity [Masashi Tsuda, et al., Scalusamides A-C, NewPyrrolidine Alkaloids from the Marine-Derived Fungus Penicilliumcitrinum, J. Nat. Prod. 2005, 68, 273-276].

Another example of an amide is a plant-derived compound calledsarmentine, which displayed a lot of bioactivities. As described inapplication Ser. No. 61/227,412, Jul. 21, 2009 sarmentine was firstisolated from the fruit of Piper sarmentosum in 1987 [Likhitwitayawuid,K., Ruangrungsi, N, Lange, G. and Decicco, C., Structural Elucidationand Synthesis of New Components isolated from Piper Samentosum,Tetrahedron 1987 (43) 3689-3694] and also from Piper nigrum in 1988[Kiuchi, F., Nakamura, N., Tsuda, Y., Kondo, K. and Yoshimura, H.Studies on Crude Drugs Effective on Visceral Larva Migrans. IV.Isolation and Identification of Larvicidal Principles in Pepper Chemicaland Pharmaceutical Bulletin 1988(36):2452], and first synthesized in1995 [Bernabeu, M., Chinchilla, R. and Najera, C.,(2E,4E)-5-Tosyl-2,4-pentadienamides: New Dienic Sulfones for theStereoselective Synthesis of (2E,4E)-Dienamides, Tetrahedron Letter,1995 (36)3901-3904]. Sarmentine has been found to act as an in vivo skinantioxidant protecting photoaged skin [Cornacchione, S.; Sadick, N. S.;Neveu, M.; Talbourdet, S.; Lazou, K.; Viron, C.; Renimel, I.; de Quéral,D.; Kurfurst, R.; Schnebert, S.; Heusele, C.; André, P.; Perrier E. Invivo skin antioxidant effect of a new combination based on a specificVitis vinifera shoots extract and a biotechnological extract. J. Drugsin Dermatol. 2007, 6S, 8-13], display antiplatelet aggregation activity[Li, C. Y.; Tsai, W.; Damu, A. G.; Lee, E. J.; Wu, T. S.; Dung. N. X.;Thang, T. D.; Thanh, L. Isolation and identification of antiplateletaggregatory principles from the leaves of Piper lolot, J. Agric. FoodChem. 2007, 55, 9436-9442], have antiplasmodial and antimycobacterialactivities [Tuntiwachwuttikul, P.; Phansa, P.; Pootaeng-on, Y.; Taylor,W. C. Chemical constituents of the roots of Piper Sarmentosum, Chem.Pharm. Bull. 2006, 54, 149-151] and antituberculosis activity[Rukachaisirikul, T.; Siriwattanakit, P.; Sukcharoenphol, K.; Wongvein,C.; Ruttanaweang, P.; Wongwattanavuch, P.; Suksamrarn, A. Chemicalconstituents and bioactivity of Piper sarmentosum, J. Ethnopharmacol.,2004, 93, 173-176]. Sarmentine is used as a solubilizer of hydrophobiccompounds in cosmetics and pharmaceuticals (Stephen, T.; Andrew, H.Compositions comprising macromolecular assembles of lipid surfactant,PCT Publication No. WO/2008/065451). Application Ser. No. 61/227,412,Jul. 21, 2009 further discloses that sarmentine and its analogs may beused to control plant pests.

BRIEF SUMMARY OF THE INVENTION

This invention is directed to the compounds, compositions and methodsfor controlling molluscs, particularly members of the Gastropoda and/orBivalvia classes and more particularly mussels, snails and slugs. Theinvention is directed to isolated compounds obtainable or derived from(a) microorganism, particularly, Pseudomonas species, more particularly,Pseudomonas fluorescens or alternatively, an organism having theidentifying characteristics of Pseudomonas ATCC 55799; (b) is toxic to amember of a class of molluscs selected from the group consisting ofBivalvia, particularly, mussels (e.g., Dreissana sp.) and/or Gastropoda,particularly, snails, which includes but is not limited to aquaticsnails (e.g., Biomphalaria sp.) and garden snails, including but notlimited to brown garden snails, white garden snails (e.g., Cantareussp., Cornu sp., Theba sp.), and/or slugs, including but not limited togray garden slug (e.g., Deroceras sp.), the banded or three-band slug(e.g., Lehmannia sp.), the tawny slug (e.g., Limacus sp.), and thegreenhouse slug (e.g., Milax sp.) and (c) has a molecular weightselected from the group consisting of: about 540-550 and about 1280-1335as determined by Liquid Chromatography/Mass Spectroscopy (LC/MS). Thesecompositions may be formulated into compositions which may be used tocontrol molluscs, particularly members of the Gastropoda and/or Bivalviaclasses and more particularly mussels, snails and slugs. In oneembodiment, the compound: (a) is obtainable from a microorganism,particularly a Pseudomonas sp.; (b) is toxic to a member of a class ofmolluscs selected from the group consisting of Bivalvia, particularly,mussels (e.g., Dreissana sp.) and/or Gastropoda, particularly, snails,which includes but is not limited to aquatic snails (e.g., Biomphalariasp.) and garden snails, including but not limited to brown gardensnails, white garden snails (e.g., Cantareus sp., Cornu sp., Theba sp.),and/or slugs, including but not limited to gray garden slug (e.g.,Deroceras sp.), the banded or three-band slug (e.g., Lehmannia sp.), thetawny slug (e.g., Limacus sp.), and the greenhouse slug (e.g., Milaxsp.); (c) has a molecular weight of about 1280-1310 and moreparticularly, 1295 as determined by Liquid Chromatography/MassSpectroscopy (LC/MS); (d) has ¹H NMR values of δ 9.25, 8.36, 8.06, 7.82,7.71, 7.52, 7.45, 6.82, 6.36, 6.08, 5.42, 5.39, 5.30, 5.14, 4.68, 4.42,4.31, 4.16, 4.11, 4.07, 3.95-3.86, 3.83, 3.72, 3.66, 3.53, 3.48, 3.37,3.17, 3.06, 2.56, 2.53, 2.45, 2.32, 2.21, 2.02, 1.96, 1.84, 1.72, 1.65,1.61, 1.51, 1.48-1.37, 1.32, 1.12, 0.94, 0.91, 0.68; (d) has a HighPressure Liquid Chromatography (HPLC) retention time of about 50-55minutes, more specifically about 52 minutes and even more specificallyabout 51.66 min on a reversed phase C-18 HPLC (e.g., Thermo Scientific,Hydersil Gold, 100×10 mm) column using a water:acetonitrile (CH₃CN) witha gradient solvent system (0-10 min; 30-40% aqueous CH₃CN, 10-20 min;40-60% aqueous CH₃CN, 20-60 min; 60-80% aqueous CH₃CN, 60-65 min;80-100% aqueous CH₃CN) at 2.5 mL/min flow rate and UV detection of 210nm.

In another embodiment, the compound has the following characteristics:(a) is obtainable from a microorganism, particularly a Pseudomonas sp.;(b) is toxic to a member of a class of molluscs selected from the groupconsisting of Bivalvia, particularly, mussels (e.g., Dreissana sp.)and/or Gastropoda, particularly, snails, which includes but is notlimited to aquatic snails (e.g., Biomphalaria sp.) and garden snails,including but not limited to brown garden snails, white garden snails(e.g., Cantareus sp., Cornu sp., Theba sp.), and/or slugs, including butnot limited to gray garden slug (e.g., Deroceras sp.), the banded orthree-band slug (e.g., Lehmannia sp.), the tawny slug (e.g., Limacussp.), and the greenhouse slug (e.g., Milax sp.); (c) has a molecularweight of about 1310-1335 and more particularly, 1321 as determined byLC/MS; (d) has a HPLC retention time of about 55-60 minutes, moreparticularly about 60 minutes and even more particularly 59.61 min on areversed phase C-18 (Thermo Scientific, Hydersil Gold, 100×10 mm) HPLCcolumn using an acetonitrile:water gradient using a water:acetonitrile(CH₃CN) with a gradient solvent system (0-10 min; 30-40% aqueous CH₃CN,10-20 min; 40-60% aqueous CH₃CN, 20-60 min; 60-80% aqueous CH₃CN, 60-65min; 80-100% aqueous CH₃CN) at 2.5 mL/min flow rate and UV detection of210 nm. In yet another embodiment, the invention is directed to anisolated compound having the following characteristics (a) is obtainablefrom a microorganism, particularly, a Pseudomonas sp.; (b) is toxic to amember of a class of molluscs selected from the group consisting ofBivalvia, particularly, mussels (e.g., Dreissana sp.) and/or Gastropoda,particularly, snails, which includes but is not limited to aquaticsnails (e.g., Biomphalaria sp.) and garden snails, including but notlimited to brown garden snails, white garden snails (e.g., Cantareussp., Cornu sp., Theba sp.), and/or slugs, including but not limited togray garden slug (e.g., Deroceras sp.), the banded or three-band slug(e.g., Lehmannia sp.), the tawny slug (e.g., Limacus sp.), and thegreenhouse slug (e.g., Milax sp.); (c) has a molecular weight of about540-550 and more particularly, about 546 as determined by LC/MS; (d) hasan HPLC retention time of about 50-55 minutes, more particularly, about52 minutes and even more particularly, about 51.54 min on a reversedphase C-18 HPLC column (Phenomenex, luna C 18(2) 10μ, 100 Å Axia,A250×30 mm) using a water:acetonitrile gradient solvent system (0-10min; 35-45% aqueous CH₃CN, 10-20 min; 45-60% aqueous CH₃CN, 20-50 min;60-85% aqueous CH₃CN, 50-60 min; 85-100% aqueous CH₃CN, 60-70 min; 100%CH₃CN) at 10 mL/min flow rate and UV detection of 210 nm.

The invention is further directed to a method for obtaining thecompound(s) of the present invention comprising

(a) obtaining a suspension of cells derived from a Pseudomonas speciesand(b) isolating the compound by chromatographic methods from saidsuspension

The invention is further directed to compositions comprising saidcompounds as well as a composition comprising a water:acetonitrilesolvent system (0-10 min; 35-45% aqueous CH₃CN, 10-20 min; 45-60%aqueous CH₃CN, 20-50 min; 60-85% aqueous CH₃CN, 50-60 min; 85-100%aqueous CH₃CN, 60-70 min; 100% CH₃CN) at 10 mL/min flow rate and UVdetection of 210 nm fraction obtainable from a Pseudomonas species cellsuspension by HPLC with a retention time of about 45-50 min, saidfraction comprising at least two compounds that (a) are toxic to amember of a class of molluscs selected from the group consisting ofBivalvia, particularly, mussels (e.g., Dreissana species) and/orGastropoda, particularly, snails, which includes but is not limited toaquatic snails (e.g., Biomphalaria species) and garden snails, includingbut not limited to brown garden snails, white garden snails (e.g.,Cantareus sp., Cornu sp., Theba sp.), and/or slugs, including but notlimited to gray garden slug (e.g., Deroceras sp.), the banded orthree-band slug (e.g., Lehmannia sp.), the tawny slug (e.g., Limacussp.), and the greenhouse slug (e.g., Milax sp.); (b) have molecularweights between about 630-660 and between about 970-1000 as determinedby LC/MS.

The invention relates a method for controlling one or more molluscs in alocation where control is desired comprising introducing into saidlocation at least one of (a) a cell suspension or extract derived fromErwinia sp. cells; (b) one or more compounds, wherein said compounds arelactone, lactam, carbamate, carboxylic acid and/or amide compounds orcomposition comprising said compounds, with the proviso that saidcompounds are not gamma-octalactone, gamma-nonalactone,gamma-decanolactone, gamma-undecalactone, N-cyclpentylcinnamamide,N-(trans-cinnamoyl)pyrrolidine, N-(trans-Cinnamoyl)piperidine andN-(trans-Cinnamoyl)hexamethyleneimine, 4-hydroxydodecanoic acid anddodecanoic acid and with the proviso that the composition is not aPseudomonas culture, extract or suspension; (c) one or more compoundsobtainable or derived from (i) Pseudomonas species, (ii) is toxic to amember of a class of molluscs selected from the group consisting ofBivalvia, particularly, mussels (e.g., Dreissana sp.) and/or Gastropoda,particularly, snails, which includes but is not limited to aquaticsnails (e.g., Biomphalaria sp.) and garden snails, including but notlimited to brown garden snails, white garden snails (e.g., Cantareussp., Cornu sp., Theba sp.), and/or slugs, including but not limited togray garden slug (e.g., Deroceras sp.), the banded or three-band slug(e.g., Lehmannia sp.), the tawny slug (e.g., Limacus sp.), and thegreenhouse slug (e.g., Milax sp.) and (iii) has a molecular weightselected from the group consisting of: about 540-550 and about 1280-1335as determined by Liquid Chromatography/Mass Spectroscopy (LC/MS); (d) acomposition comprising a water:acetonitrile solvent system (0-10 min;35-45% aqueous CH₃CN, 10-20 min; 45-60% aqueous CH₃CN, 20-50 min; 60-85%aqueous CH₃CN, 50-60 min; 85-100% aqueous CH₃CN, 60-70 min; 100% CH₃CN)at 10 mL/min flow rate and UV detection of 210 nm fraction obtainablefrom a Pseudomonas species cell suspension by HPLC with a retention timeof about 45-50 min, said fraction comprising at least two compounds that(i) are toxic to a member of a class of molluscs selected from the groupconsisting of Bivalvia, particularly, mussels (e.g., Dreissana sp.)and/or Gastropoda, particularly, snails, which includes but is notlimited to aquatic snails (e.g., Biomphalaria sp.) and garden snails,including but not limited to brown garden snails, white garden snails(e.g., Cantareus sp., Cornu sp., Theba sp.), and/or slugs, including butnot limited to gray garden slug (e.g., Deroceras sp.), the banded orthree-band slug (e.g., Lehmannia sp.), the tawny slug (e.g., Limacussp.), and the greenhouse slug (e.g., Milax sp.); (ii) have molecularweights between about 630-660 and between about 970-1000 as determinedby LC/MS, in amounts effective to control said molluscs in saidlocation. This control may in one embodiment be achieved by inducingdeath in one or more molluscs comprising contacting said molluscs withthe compounds set forth above. The molluscs may be contacted in a bodyof water or solid surface. Similarly, the invention is directed to theuse of the above-referenced compounds, suspensions and compositions forformulating a composition for use in controlling mollusks, such asGastropoda and Bivalvia in a location.

In a related aspect, the invention further relates to compositions forcontrolling one or more molluscs, particularly mussels and/or snails(e.g., white and/or brown garden snails, aquatic snails) and/or slugs ina location where control is desired and/or inducing death in one or moremolluscs, particularly mussels and/or snails (e.g., white and/or browngarden snails, aquatic snails) and/or slugs in said location comprisingone or more lactones, lactams, carbamates, carboxylic acids and/oramides, again with the proviso that said compound is notgamma-octalactone, gamma-nonalactone, gamma-decanolactone,gamma-undecalactone, N-cyclpentylcinnamamide,N-(trans-cinnamoyl)pyrrolidine, N-(trans-Cinnamoyl)piperidine andN-(trans-Cinnamoyl)hexamethyleneimine, 4-hydroxydecanoic acid anddecanoic acid and with the proviso that the composition is not aPseudomonas culture, extract or suspension.

In a particular embodiment, the invention is directed to a method forcontrolling one or more molluscs, particularly mussels and/or snails(e.g., white and/or brown garden snails, aquatic snails) and/or slugs,said method comprising the steps of:

(a) preparing a cell suspension or extract derived from Erwinia sp.cells; and

(b) introducing said suspension or extract into a location where controlis desired in an amount effective to control said molluscs.

Erwinia extracts may contain active ingredients set forth above, such aslactones and amides. Similarly the cell suspension or extract derivedfrom Erwinia sp. cells may be formulated into compositions for use incontrolling molluscs, particularly a class of molluscs selected from thegroup consisting of Bivalvia, particularly, mussels (e.g., Dreissanasp.) and/or Gastropoda, particularly, snails, which includes but is notlimited to aquatic snails (e.g., Biomphalaria sp.) and garden snails,including but not limited to brown garden snails, white garden snails(e.g., Cantareus sp., Cornu sp., Theba sp.), and/or slugs, including butnot limited to gray garden slug (e.g., Deroceras sp.), the banded orthree-band slug (e.g., Lehmannia sp.), the tawny slug (e.g., Limacussp.), and the greenhouse slug (e.g., Milax sp.).

The invention is further directed to a composition comprising at leastone or more substances effective for controlling one or more molluscs,particularly a class of molluscs selected from the group consisting ofBivalvia, particularly, mussels (e.g., Dreissana sp.) and/or Gastropoda,particularly, snails, which includes but is not limited to aquaticsnails (e.g., Biomphalaria sp.) and garden snails, including but notlimited to brown garden snails, white garden snails (e.g., Cantareussp., Cornu sp., Theba sp.), and/or slugs, including but not limited togray garden slug (e.g., Deroceras sp.), the banded or three-band slug(e.g., Lehmannia sp.), the tawny slug (e.g., Limacus sp.), and thegreenhouse slug (e.g., Milax sp.), and optionally an inert materialpreferably for use in controlling one or more mollucs. The substance maybe derived from chlorine or a Pseudomonas species, more particularlyderived from Pseudomonas fluorescens or alternatively an organism (e.g.,a Pseudomonas strain) having the identifying characteristics ofPseudomonas ATCC 55799. In another particular embodiment, thecomposition may comprise a substance that is a cell suspension derivedfrom a Pseudomonas species (e.g., P. fluorescens) and even in a moreparticular embodiment, the cell suspension may comprise cells having thetoxin producing characteristics of Pseudomonas ATCC 55799. In yetanother particular embodiment, the substances in said composition may beone or more toxins derived from isolated from a Pseudomonas species oralternatively derived from an organism having the identifyingcharacteristics of Pseudomonas ATCC 55799. The composition mayalternatively comprise the compounds used in the method of the presentinvention set forth above as well as the compounds of the presentinvention set forth above and may be used to control a member of aGastropoda and Bivalvia class. The inert material may be a clay mineral(kaolinite, smectite, attapulgite). The invention is further directed toa method for controlling one or more molluscs, particularly, musselsand/or snails (e.g, aquatic, garden snails and/or slugs in a locationwhere control is desired comprising introducing in said location asubstance effective for controlling said molluscs and optionally one ormore inert materials in amounts effective to control said molluscs insaid location containing said molluscs. In particular, the substance forcontrolling said molluscs is present in an amount effective to result inat least about a 20% mortality relative to untreated control, typicallyabout 50-95% and said inert material is present in an amount sufficientor effective to increase mortality rate of said substance forcontrolling said molluscs at least about 20%, typically 25-40%. In aparticular embodiment, the inert material is introduced into saidlocation prior to introduction of the substance for controlling saidmolluscs; in a more particular embodiment, the inert material isintroduced at least about one hour prior to the introduction of thesubstance. In another particular embodiment, the inert material isintroduced into the location simultaneously with the substance forcontrolling molluscs set forth above, particularly mussels, snailsand/or slugs.

In a related aspect, the invention is directed to the use of an inertmaterial for increasing the efficacy of one or more substances forcontrolling one or more molluscs, particularly a class of molluscsselected from the group consisting of Bivalvia, particularly, mussels(e.g., Dreissana sp.) and/or Gastropoda, particularly, snails, whichincludes but is not limited to aquatic snails (e.g., Biomphalaria sp.)and garden snails, including but not limited to brown garden snails,white garden snails (e.g., Cantareus sp., Cornu sp., Theba sp.), and/orslugs, including but not limited to gray garden slug (e.g., Derocerassp.), the banded or three-band slug (e.g., Lehmannia sp.), the tawnyslug (e.g., Limacus sp.), and the greenhouse slug (e.g., Milax sp.), ina location where control is desired. The location may be a liquid (e.g.,a body of water or paint) or solid surface, such as plastic, concrete,wood, fiberglass, pipes made of iron and polyvinyl chloride, surfacescovered with coating materials and/or paints. In particular, theinvention is directed to a method for increasing the efficacy of one ormore substances for controlling one or more of said molluscs,particularly a class of molluscs selected from the group consisting ofBivalvia, particularly, mussels (e.g., Dreissana sp.) and/or Gastropoda,particularly, snails, which includes but is not limited to aquaticsnails (e.g., Biomphalaria sp.) and garden snails, including but notlimited to brown garden snails, white garden snails (e.g., Cantareussp., Cornu sp., Theba sp.), and/or slugs, including but not limited togray garden slug (e.g., Deroceras sp.), the banded or three-band slug(e.g., Lehmannia sp.), the tawny slug (e.g., Limacus sp.), and thegreenhouse slug (e.g., Milax sp.), comprising introducing in a locationwhere control is desired one or more inert materials in amountseffective to increase efficacy of said substance when introduced in saidlocation. In a particular embodiment, these inert materials increasesthe efficacy of said substances at least about 20%.

Further, the invention relates to an antifouling paint comprising anantivegative, biocidal effective amount of the compositions andcompounds of the present invention in a paint carrier. The inventionfurther relates to the use of the compounds and compositions of thepresent invention in formulating such an antifouling paint.

BRIEF DESCRIPTION OF THE FIGURES

FIGS. 1 a and 1 b shows structures of natural products used in themethod of the present invention.

FIG. 2 shows the scheme for isolating the active fractions.

FIG. 3 shows one schematic representation of the purification scheme forobtaining the compounds of the present invention from Pseudomonas cellculture.

FIG. 4 shows development of mortality over time for mussels treated withclay and P. fluorescens biopesticide product in a biobox.

DETAILED DESCRIPTION OF THE INVENTION

Where a range of values is provided, it is understood that eachintervening value, to the tenth of the unit of the lower limit unlessthe context clearly dictates otherwise, between the upper and lowerlimit of that range and any other stated or intervening value in thatstated range is encompassed within the invention. The upper and lowerlimits of these smaller ranges may independently be included in thesmaller ranges is also encompassed within the invention, subject to anyspecifically excluded limit in the stated range. Where the stated rangeincludes one or both of the limits, ranges excluding either both ofthose included limits are also included in the invention.

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this invention belongs. Although any methods andmaterials similar or equivalent to those described herein can also beused in the practice or testing of the present invention, the preferredmethods and materials are now described.

It must be noted that as used herein and in the appended claims, thesingular forms “a,” “and” and “the” include plural references unless thecontext clearly dictates otherwise.

As defined herein, “controlling mussels” means controlling the eggs,larvae, veligers and post-veligers of the mussel by killing or disablingthem so that they cannot colonize in a give location.

As defined herein, “derived from” means directly isolated or obtainedfrom a particular source or alternatively having identifyingcharacteristics of a substance or organism isolated or obtained from aparticular source.

As used hereafter, the term “alkyl” refers to a saturated hydrocarbonradical which may be straight-chain or branched-chain (e.g., ethyl,isopropyl, t-amyl, or 2,5-dimethylhexyl, etc.). This definition appliesboth when the term is used alone and when it is used as part of acompound term.

The terms “cycloalkyl” and “cycloalkenyl” refer to a saturatedhydrocarbon ring and includes bicyclic and polycyclic rings. Similarly,cycloalkyl and cycloalkenyl groups having a heteroatom (e.g., N, O, orS) in place of a carbon ring atom may be referred to as“heterocycloalkyl”, “heterocyclyl,” and “heterocycloalkylene,”respectively.

The term “alkenyl” as used herein refers to an alkyl group as describedabove which contains one or more sites of unsaturation that is a doublebond. Similarly, the term “alkynyl” as used herein refers to an alkylgroup as described above which contains one or more sites ofunsaturation that is a triple bond.

The term “alkoxy” refers to an alkyl radical as described above whichalso bears an oxygen substituent which is capable of covalent attachmentto another hydrocarbon radical (such as, for example, methoxy, ethoxy,aryloxy, and t-butoxy).

The term “aryl” refers to an aromatic carbocyclic substituent which maybe a single ring or multiple rings which are fused together, linkedcovalently or linked to a common group such as an ethylene or methylenemoiety. Similarly, aryl groups having a heteroatom (e.g., N, O, or S) inplace of a carbon ring atom are referred to as “heteroaryl.”

The terms “arylalkyl,” “arylalkenyl,” and “aryloxyalkyl” refer to anaryl radical attached directly to an alkyl group, an alkenyl group, oran oxygen atom which is attached to an alkyl group, respectively. Forbrevity, aryl as part of a combined term as above is meant to includeheteroaryl as well.

The term “hetero” as used in a “heteroatom-containing alkyl group”(i.e., a “heteroalkyl” group) or a “heteroatom-containing aryl group”(i.e., a “heteroaryl” group) refers to a molecule, linkage, orsubstituent in which one or more carbon atoms are replaced with an atomother than carbon, e.g., nitrogen, oxygen, sulfur, phosphorus, orsilicon.

As defined herein, “derived from” and “obtainable from” means directlyisolated or obtained from a particular source or alternatively havingidentifying characteristics of a substance or organism isolated orobtained from a particular source. These terms are used interchangeablythroughout the specification.

As defined herein, an “isolated compound” is essentially free of othercompounds or substances, e.g., at least about 20% pure, preferably atleast about 40% pure, more preferably about 60% pure, even morepreferably about 80% pure, most preferably about 90% pure, and even mostpreferably about 95% pure, as determined by analytical methods,including but not limited to chromatographic methods, electrophoreticmethods.

Compounds

The compounds used in the compositions and methods of the presentinvention may be members of the following three families.

Family I Compounds

In a particular embodiment, family I possesses following chemicalstructures:

Where X includes, but is not limited to carbon, sulfur, phosphorus; Yincludes, but is not limited to sulfur, oxygen; A and M include, but arenot limited to carbon, oxygen, nitrogen, sulfur and n is 1 to 21 Where(R)_(z) represents number Z of the number of substituents on the group Ron the ring. R and the substituents on R may be a hydrogen, hydroxyl,alkyl hydroxyl, akenyl hydroxyl, alkynyl hydroxyl, alkyloxy,alkenyloxyl, alkynyloxy, cycloalkyl, cycloalkenyl, alkyl, alkenyl,alkynyl, heterocyclyl, heteroaryl, aromatic, aryl group, NH-substituted,or N,N-substituted group or any other substituted group. The length ofthe one of the substituted R chains can be from 1 to 25 atoms, thepreferred length will be from 7 to 17 atoms; The number Z can be 0, 1,2, 3 until n+2, preferred z=0, 1, 2, 3.

In a particular embodiment, the compound may be derived from Pseudomonasfluorescens and has a hydroxylated unsaturated fatty acid lactonestructure comprising at least one lactone moiety which is a 5 memberedγ-lactone, at least one unsaturated moiety and at least one alcoholgroup; a molecular weight from 285 to about 310 in the core structure;at least 15 carbons and at least 3 oxygens. In a more particularembodiment, the compound may have the structure

wherein: X are each independently —O, —NR₁, or —S, wherein R₁ is —H orC₁-C₆alkyl; n=0 to 15, R₂ to R₄ are each independently —H, alkyl,substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substitutedalkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, substituted heterocyclic, cycloalkyl, substitutedcycloalkyl, alkoxy, substituted alkoxy, thioalkyl, substitutedthioalkyl, hydroxy, halogen, amino, amido, carboxyl, —C(O)H, acyl,oxyacyl, carbamate, sulfonyl, sulfonamide, or sulfuryl; m=double bond ortriple bond. In yet another particular embodiment, Y and M are oxygen, Aand X are carbon and n is 2 or 3, R is a C7 or C8 alkyl and z is 0,wherein when n is 2 and R is a C7 alkyl, R is attached to A.

In an even another particular embodiment, Family I compounds may be thecompounds set forth in 1 to 28 (FIGS. 1 a and 1 b). These are fromeither natural materials or compounds obtained from commercial sourcesor by chemical synthesis. Natural sources of Family I compounds include,but are not limited to plants, corals, microorganisms, sponges andanimals. In a more particular embodiment, plants which include theFamily I compounds include but are not limited to, or alternatively,Family I compounds may be derived from species such as Myoporumbontioides (compound 14) [Moe Kanemoto, et al., Chlorine-containingiridoid and iridoid glucoside, and other glucosides from leaves ofMyoporum bontioides, Phytochemistry 69 (2008) 2517-2522], Micromelumhirsutum (compound 18) [Ma, G. Y. et al. anti-tuberculosis constituentsfrom the stem bark of Micromelum hirsutum, Planta Med. 2005, 71,261-267], Family I compounds may also be derived from microorganismsincluding but not limited to Antrodia camphorate (compounds 4, 5) [Shan,Y. Y. et al., Chemical constituents of Antrodia camphorata submergedwhole broth, Natural Product Research, 2008, 22 (13) 1151-1157],Saccharomyces cerevisiae (compound 2) [Gocho, S. et al.Biotransformation of oleic acid to optically active γ-dodecalactone,Biosci. Biotech. Biochem. 1995, 59 (8) 1571-1572], Mesorhizobium sp.(compounds 2, 17) [Wei, G. H. et al., Rhizobialide: A New StearolactoneProduced by Mesorhizobium sp. CCNWGX022, a Rhizobial Endophyte fromGlycyrrhiza uralensis, Chemistry and Biodiversity, 2007, 4, 893-898],Ophiostoma piliferum (compound 16), [Wei, G. H. et al., Rhizobialide: ANew Stearolactone Produced by Mesorhizobium sp. CCNWGX022, a RhizobialEndophyte from Glycyrrhiza uralensis, Chemistry and Biodiversity, 2007,4, 893-898], Streptomyces sp. (compound 8) [Khaled A. Shaaban, MohamedShaaban, Petrea Facey, Serge Fotso, Holm Frauendorf, Elisabeth Helmke,Armin Maier, Heinz H. Fiebig, Hartmut Laatsch, Electrospray IonizationMass Spectra of Piperazimycins A and B and γ-Butyrolactones from aMarine-derived Streptomyces sp. J. Antibiot. 61(12): 736-746, 2008],Macrophomina phaseolzna (compounds 9, 10 & 15) [Shashib, Mahat et al.,structure and stereochemistry of phaseolinic acid: a new acid fromMacrophomina phaseolzna, Journal of Natural products, 1987, 50 (2)245-247], Sporidiobolus salmonicolor (compounds 1, 3) [Laurent Dufosse,et al., Chirality of the γ-Lactones Produced by Sporidiobolussalmonicolor Grown in Two Different Media, Chirality, 1997, 667-671] andStreptomyces (compound 7) [Shohei Sakuda, et al., Biosynthetic Studieson Virginiae Butanolide A, a Butyrolactone Autoregulator fromStreptomyces. Part 2, Preparation of Possible Biosynthetic Intermediatesand Conversion Experiments in a Cell-free System. J. Chem. Soc. PerkinTrans. 11993, 2309-2315].

In an additional particular embodiment, Family I compounds may bederived from sponges such as Haliclona n. sp (compounds 26, 27 & 28)[Richard J. Clark, Mary J. Garson, and John N. A. Hooper, AntifungalAlkyl Amino Alcohols from the Tropical Marine Sponge Haliclona n. sp. J.Nat. Prod. 2001, 64, 1568-1571], Axinellas sp (compound 25) [Miller, W.F. Tinto, J.-P. Yang, S. McLean and W. F. Reynolds, Axinellamide, a newalkaloid from the marine sponge Axinellas sp. Tetrahedron Lett., 1995,36, 5851], Plakortis nigra (compounds 19-20) [Joel S. Sandler, et al.,Cytotoxic β-Carbolines and Cyclic Peroxides from the Palauan SpongePlakortis nigra, J. Nat. Prod. 2002, 65, 1258-1261] and Irciniaformosana (compounds 21-24) [Shen, Y. C. et al., Novel linearC22-sesterterpenoids from sponge Ircinia formosana, Tetrahedron Letters47 (2006) 4007-4010]. Compounds 26-28 are examples of carbamates.

In another particular embodiment, Family I compounds may be derived fromcorals including but not limited to Sarcophyton trocheliophorum andLithophyton arboreturn (compounds 11 & 13) [Tomas Rezanka, et al.,γ-lactones from the soft corals Sarcophyton trocheliophorum andLithophyton arboreturn, Tetrahedron, 2001, 57, 8743-8749]. In yetanother particular embodiment, insects which include the Family Icompounds may be derived from insects including but not limited toFemale Japanese Beetle Sex Pheromone (compound 12) [J. H. Tumlinson,Identification of the Female Japanese Beetle Sex Pheromone Inhibition ofMale Response by an Enantiomer, Science, 1977, 197, 789-792] and insecttoxins (compound 6) [John A. Findlay, et al., Insect toxins from spruceendophytes, Can. J. Chem. 2003, 81, 284-292].

Family I compounds may also include but are not limited togamma-dodecalactone, delta-tridecalactone, piliferolide A andalpha-heptyl-gamma-butyrolactone set forth in the Examples. These may beobtained by synthetic methods using procedures known in the art or fromcommercial sources.

Family II Compounds

In another particular embodiment, family II possesses following chemicalstructures:

Where X is carbon; Y is oxygen; A, B and M are carbon, oxygen, nitrogen,sulfur or other atoms and n is 1 to 21.

Where (R)z represents number Z of the number of substituents on thegroup R on the ring. R and the substituents on R may be a hydrogen,hydroxyl, alkyl hydroxyl, akenyl hydroxyl, alkynyl hydroxyl, alkyloxy,alkenyloxyl, alkynylxoy, cycloalkyl, cycloalkenyl, alkyl, alkenyl,alkynyl, heterocyclyl, heteroaryl, aromatic, aryl group, NH-substituted,or N,N-substituted group or any other substituted group. The length ofthe one of the substituted R chain can be from 1 to 25 atoms, with thepreferred length being from 7 to 17 atoms. The number Z can be 0, 1, 2,3 until n+2, preferred z=0, 1, 2, 3.

In a particular embodiment, Family II compounds such as compounds from29 to 36 and 44 (see FIGS. 1 a and 1 b) may be derived from naturalsources, chemical synthesis or commercial sources. Natural sources ofFamily II compounds include, but are not limited to plants, corals,microorganisms, sponges and animals. In a particular embodiment,examples of such plants include, but are not limited the followingspecies such as Heteroplexis micocephala (compounds 30, 31, 32 & 33)[Fan, X. N., et al., Chemical Constituents of Heteroplexis micocephala.J. Nat. Prod. 2009, 72, 1184-1190] and Iryanthera species (compound 34)[Vieira, P. C., et al., γ-Lactones from Iryanthera species,Phytochemistry, 1983, 22 (3) 711-713] and Litse verticillata (compound44) [Mang, H. J. et al., sesquiterpenes and butenolides, naturalanti-HIV constituents from Litse verticillata, Planta Med, 2005, 71,452-457]. In a more particular embodiment, sources microorganisms whichinclude the Family II compounds include, but are not limited thefollowing species such as Streptomyces rishiriensis A-5969 (compound 29)[Yumiko Itoh, Hiroshi Shimura, Mayumito, NaoHaru Watanabe, MichioYamagishi, Masaharu Tamai and Kazunori Hanada, novel hepatoprotective7-lactone, MH-031, Discovery, Isolation, Physical-Chemical propertiesand structural elucidation, The Journal of antibiotics, 1991, 44 (8)832-837. In a more particular embodiment, corals which include theFamily II compounds include, but are not limited to the followingspecies such as Pterogorgia anceps (compound 35) [Guo, Y. W. et al.,Three New Butenolide Lipids from the Caribbean Gorgonian Pterogorgiaanceps, J. Nat. Prod. 1999, 62, 1194-1196; Manuel Lorenzo et al., ¹³CNMR-Based Empirical Rules to Determine the Configuration of Fatty AcidButanolides. Novel γ-Dilactones from Pterogorgia spp, Organic Letters, 8(22) 5001-5004] and Pterogorgia citrine (compound 36) [Abimael D.Rodriguez et al., further butenolides from the Caribbean octocoralPterogorgia citrine, Journal of Natural Products, 1994, 57(3) 339-347].

Family III Compounds

In another particular embodiment, family III compounds possess thefollowing chemical structure:

Wherein X is carbon; Y is oxygen; Z is hydrogen, hydroxyl, alkenylhydroxyl, alkynyl hydroxyl, alkyl, alkenyl, alkynyl, heterocyclyl,aromatic, aryl group, NH-substituted, or N,N-substituted group or anyother substituted group.

Wherein R is alkenyl hydroxyl, alkynyl hydroxyl, alkyl, alkenyl,alkynyl, heterocyclyl, aromatic, aryl group, NH-substituted, orN,N-substituted group or any other substituted group. The length of Rchain can be from 1 to 50, preferred from 7 to 17.

In a particular embodiment, Family III compounds such as compounds from37 to 43 (FIGS. 1 a and 1 b) may be derived from natural or commercialsources or by chemical synthesis. Natural sources of Family IIIcompounds include, but are not limited to plants, corals,microorganisms, sponges and animals. In a more particular embodiment,plants sources include, but are not limited to Piper spp (compound 43)[Likhitwitayawuid, K., Ruangrungsi, N, Lange, G. and Decicco, C.,Structural Elucidation and Synthesis of New Components isolated fromPiper Samentosum, Tetrahedron 1987 (43) 3689-3694; Kiuchi, F., Nakamura,N., Tsuda, Y., Kondo, K. and Yoshimura, H. Studies on Crude DrugsEffective on Visceral Larva Migrans. IV. Isolation and Identification ofLarvicidal Principles in Pepper Chemical and Pharmaceutical Bulletin1988(36):2452]. In a more particular embodiment, corals include, but arenot limited to Plexaura flava (compound 42) [B. N. Ravi, et al., Lipidand Terpenoid Metabolites of the Gorgonian Plexaura flava, Aust. J.Chem., 1982, 35, 105-12] and In a more particular embodiment,microorganisms which include the Family III compounds include, but arenot limited the following species such as Lyngbya majuscula andSchizothrix calcicola (compound 39, 40) [George G. Harrigan, et al.,Tumonoic Acids, Novel Metabolites from a Cyanobacterial Assemblage ofLyngbya majuscula and Schizothrix calcicola, J. Nat. Prod. 1999, 62,464-467], Pseudomonas aeruginosa (compound 41) [Michael, K. Winson., etal. Multiple N-acyl-L-homoserine lactone signal molecules regulateproduction of virulence determinants and secondary metabolites inPseudomonas aeruginosa, Proc. Natl. Acad. Sci. USA, 1995, 92,9427-9431], Erwinia carotovora (compound 37) [Gu″nter Brader, SolveigSjo″blom, Heidi Hyytia″inen, Karen Sims-Huopaniemi, and E. Tapio Palva,Altering Substrate Chain Length Specificity of an Acylhomoserine LactoneSynthase in Bacterial Communication, The Journal of BiologicalChemistry, 2005, 280(11) 10403-10409] and Photobacterium phosphoreum(compound 38) [L. R. Flodgaard, P. Dalgaard, J. B. Andersen, K. F.Nielsen, M. Givskov, and L. Gram, Nonbioluminescent Strains ofPhotobacterium phosphoreum produce the Cell-to-Cell Communication SignalN-(3-Hydroxyoctanoyl)homoserine Lactone, Applied and EnvironmentalMicrobiology, 2005, 71(4), 2113-2120].

In yet another particular embodiment, the family III compounds may be asarmentine analog having the following structure:

Wherein R1 is an alkyl, alkenyl, alkynyl, heterocyclyl, aromatic, arylgroup, NH-substituted, or N,N-substituted group and the length of R1chain is from 4 to 20 atoms, and preferably from 6 to 12 atoms.

Wherein R2 and R3 are alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl,aromatic, arylalkyl, heterocyclyl or heteroaryl; or alternativelyR2+R3+N can be an N-containing heterocyclic moiety, Wherein when R2+R3+Nis an N-containing heterocyclic moiety, R1 is an alkyl, alkenyl,alkynyl, heterocyclyl, NH-substituted, or N,N-substituted group.

In a most particular embodiment, the sarmentine analog isN-Cyclopentyldecanamide, N-(Decanoyl)pyrrolidine,N-(Decanoyl)piperidine, N-(Decanoyl)hexamethyleneimine,N-Cyclopentyldecenamide, (N-(Decenoyl)pyrrolidine,N-(Decenoyl)piperidine, N-(Decenoyl)hexamethyleneimine andN-(Decenoyl)piperidine.

The sarmentine analogs may be obtained using procedures known in the artwhich may include but is not limited to those set forth in applicationSer. No. 61/227,412, filed Jul. 21, 2009.

In yet another particular embodiment, the compound may be derived fromPseudomonas fluorescens and characterized as having a hydroxylatedunsaturated fatty acid structure comprising at least one carboxylic acidmoiety, at least one unsaturated moiety and at least one alcohol group;molecular weight from 285 to about 310 in the core structure; at least15 carbons and at least 3 oxygens.

In a more particular embodiment of the invention, there are providedcompounds having the structure

wherein: X are each independently —OH, —NR₁, or —S, wherein R₁ is —H orC₁-C₆ alkyl; n=0 to 15, R₂ to R₄ are each independently —H, alkyl,substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substitutedalkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, substituted heterocyclic, cycloalkyl, substitutedcycloalkyl, alkoxy, substituted alkoxy, thioalkyl, substitutedthioalkyl, hydroxy, halogen, amino, amido, carboxyl, —C(O)H, acyl,oxyacyl, carbamate, sulfonyl, sulfonamide, or sulfuryl; m=double bond,triple bond. In a most specific embodiment, the compound has thestructure

Methods of Production

As noted above, the compounds and compositions of the present inventionmay be obtained, is obtainable or derived from an organism having theidentifying characteristics of a Pseudomonas species, more particularly,from an organism having the identifying characteristics of a strain ofPseudomonas fluorescens or alternatively from an organism having theidentifying characteristics of Pseudomonas fluorescens isolate, ATCC55799 as set forth in U.S. Pat. No. 6,194,194. The methods comprisecultivating these organisms and obtaining the compounds and/orcompositions of the present invention by isolating these compounds fromthe cells of these organisms.

In particular, the organisms are cultivated in a nutrient medium usingmethods known in the art. The organisms may be cultivated by shake flaskcultivation, small scale or large scale fermentation (including but notlimited to continuous, batch, fed-batch, or solid state fermentations)in laboratory or industrial fermentors performed in suitable medium andunder conditions allowing cell growth. The cultivation may take place insuitable nutrient medium comprising carbon and nitrogen sources andinorganic salts, using procedures known in the art. Suitable media areavailable may be available from commercial sources or prepared accordingto published compositions. A particular embodiment is disclosed in theexamples infra and in U.S. Pat. No. 6,194,194.

After cultivation, the cells may be concentrated and subsequentlysuspended in a buffer to obtain a cell suspension. The compounds and/orcompositions of the present invention may be extracted from thesuspension. The extract may be fractionated by chromatography.Chromatography may be assayed for toxic activity against molluscs, suchas mussels, snails (e.g., aquatic and/or garden snails) and/or slugs,using methods known in the art; one particular embodiment is disclosedin the examples, infra. This process may be repeated one or more timesusing the same or different chromatographic methods.

The compounds of the present invention may also be obtained by syntheticmethods. Alternatively, for peptide compounds, the compounds may beobtained by expressing nucleic acid sequences encoding these compoundsin a recombinant DNA host using methods known in the art.

Formulations

The composition of the present invention may comprise a chemical orbiopesticide product that is useful in controlling molluscs,particularly members of the Gastropoda and/or Bivalvia classes and moreparticularly mussels, snails and slugs. The invention is directed toisolated compounds obtainable or derived from (a) a microorganism suchas a Pseudomonas species, more particularly, Pseudomonas fluorescens oralternatively, an organism having the identifying characteristics ofPseudomonas ATCC 55799; (b) is toxic to a member of a class of molluscsselected from the group consisting of Bivalvia, particularly, mussels(e.g., Dreissana species) and/or Gastropoda, particularly, snails, whichincludes but is not limited to aquatic snails (e.g., Biomphalariaspecies) and garden snails, including but not limited to brown gardensnails, white garden snails (e.g., Cantareus species, Cornu species,Theba species), and/or slugs, including but not limited to gray gardenslug (e.g., Deroceras sp.), the banded or three-band slug (e.g.,Lehmannia sp.), the tawny slug (e.g., Limacus sp.), and the greenhouseslug (e.g., Milax sp.) and (c) has a molecular weight selected from thegroup consisting of: about 540-550 and about 1280-1335 as determined byLiquid Chromatography/Mass Spectroscopy (LC/MS). These compositions maybe formulated into compositions which may be used to control molluscs,particularly members of the Gastropoda and/or Bivalvia classes and moreparticularly mussels, snails and slugs.

Examples include but are not limited to chlorine and substances derivedfrom a Pseudomonas species as described in for example U.S. Pat. No.6,194,194. Furthermore, compounds disclosed above and used in theinvention can be made into compositions (also alternatively referred toas “formulations”) and can be formulated in any form. Non-limitingformulation examples include emulsifiable concentrates (EC), wettablepowders (WP), soluble liquids (SL), aerosols, ultra-low volumeconcentrate solutions (ULV), soluble powders (SP), microencapsulation,water dispersed granules, flowables (FL), microemulsions (ME),nano-emulsions (NE), etc. In any formulation described herein, percentof active ingredient is within a range of 0.01% to 99.99%. In aparticular embodiment, the formulations may be free of surfactants.

Examples of the inert material that may be used in the compositions ofthe present invention include, but are not limited to, inorganicminerals such as kaolin, mica, gypsum, phyllosilicates, carbonates,sulfates, or phosphates; or botanical materials such as wood products,cork, powdered corn cobs, rice hulls, peanut hulls and walnut shells. Ina particular embodiment, the inert material can be obtained or derivedfrom a clay mineral (kaolinite, smectite, attapulgite) suspended inwater at a rate of about 1 to 20 mg/liter corresponding to approximately1 to 20 NTU (normalized turbidity units). The inert materials used toenhance mussel siphoning can be applied in solid form or as a suspensionin aqueous solution, preferably water, directly to the water or thelocation (e.g., solid surface) where the mussels are treated. In aparticular embodiment, to enhance product efficacy, an inert materialsuch as clay, silt, sediment or any other material with no nutritionalvalue and with a small enough particle size can be suspended in waterprior to the treatment with a chemical or a biopesticide product.

Methods of Use

The compounds and compositions of the present invention may be used tocontrol molluscs, particularly, a member of the Gastropoda and/orBivalvia class, more particularly mussels (e.g., Dreissana species)and/or Gastropoda, particularly, snails, which includes but is notlimited to aquatic snails (e.g., Biomphalaria species) and gardensnails, including but not limited to brown garden snails, white gardensnails (e.g., Cantareus species, Cornu species, Theba species), and/orslugs, including but not limited to gray garden slug (e.g., Derocerassp.), the banded or three-band slug (e.g., Lehmannia sp.), the tawnyslug (e.g., Limacus sp.), and the greenhouse slug (e.g., Milax sp.) in abody of water or on surfaces where molluscs such as mussels, snailsand/or slugs gather or alternatively as an anti-fouling agent in paint.In the event that it is used as an antifouling agent in paint, it ispresent in an anti-vegetative, biocidally effective amount. Surfaceswhere molluscs such as mussels, snails and/or slugs include but are notlimited to plastic, concrete, wood, fiberglass, pipes made of iron andpolyvinyl chloride and surfaces covered with paints and/or coatings.Coatings may be formulated from pigments, binders, additives, and/orcarrier fluids and are preferably applied in a thin film to provideprotection or decoration to a surface. The end product (which containsthe active compound) will be used at 10-200 mg/L, more specifically at25-100 mg/L (ppm) or 25-10000 mg/kg. It will be applied either as a dryproduct or suspended in water into pipes, dam structures, holding tanks,and open waters such as streams, rivers, lakes, irrigation canals, pondsand lakes through specific application pumps and mixing systems.

In a particular embodiment, the present invention is directed to amethod for improving biopesticidal and pesticidal activity of materialsused to control invasive molluscs, particularly mussels comprising thesteps of:

-   -   1. suspension of inert material such as clay into the water to        trigger the siphoning activity for about 1-24 hours before the        chemical or biopesticide treatment    -   2. addition of a chemical or a biopesticide into the water at a        desired level

The invention is also directed to a method comprising a step ofadministering a microbial biopesticide in combination of an inertmaterial such as clay to enhance the uptake and hence, mortality ofmussels.

To activate the mussel siphoning, this clay (turbidity) treatment shouldbe carried on for about 1 to 6 hours, usually about 3-4 hours, and forabout 1 to 24 hours, typically about 14-18 hours before the treatmentwith a chemical/pesticide. Alternatively, the turbidity treatment can beapplied simultaneously with the chemical or biopesticide treatment.

According to the one embodiment of this invention, treatment ofmolluscs, such as mussels, snails and slugs can be carried out in 500-mLglass jars or in a biobox constructed of acrylic sheets. In the glassjars, aeration during treatment is provided by airflow through aquariumair stones connected to nylon tubing. In the biobox, water is constantlyflowing at a rate of 1 gallon per minute.

The materials for the turbidity treatment as well as for thechemical/biopesticide product can be mixed in the water by pipetting orvia a peristaltic pump. In bioboxes, a more uniform mixing is achievedusing a paddle mixer at the point of injection. The compositions of thepresent invention can be in a suitable form for direct application or asa concentrate or primary composition, which requires dilution with asuitable quantity of water or other diluent before application.

The effective amount of the turbidity materials will depend upon theapplication, water temperature, if applied to water, and duration of thetreatment. In general, the composition may be applied at a rate of fromabout 1 to about 20 mg per liter; preferably at a rate of from about 5to about 10 mg per liter so that the measured turbidity does not riseabove 20 NTU.

EXAMPLES

The example below is presented to describe preferred embodiments andutilities of the invention and is not meant to limit the inventionunless otherwise stated in the claims appended hereto.

Example 1 Molluscicide Studies Materials and Methods

1. Allow quagga mussels to acclimate in the small Petri dishes for 24hrs.

-   -   Pour the mussels into a Petri dish to determine if the mussels        are alive or not. Toss out the dead and empty mussels.    -   Count out 10 live/healthy mussels.    -   Put 10 live/healthy mussels in each small Petri dish with hard        water.    -   Keep a separate plate of mussels. These are the “extra mussels”        that will be used to replace dead or empty mussels after 24 hrs        in the other experimental plates.    -   Aeration is not needed due to the low volume of water (DO is        high).

2. Day of mussel treatment:

-   -   Check the mussels (Use the rubber policemen at all times when        checking the mussels. Only use the tweezers to remove dead        mussels).    -   Count to make sure there are 10 live/healthy mussels per small        Petri dish.    -   Get the sample(s) ready.    -   Dilute appropriately with hard water in a 50 ml falcon tube for        each sample. Vortex to mix prior to dosing.    -   EX: 70 ppm, 2 reps per sample. Add 34 ml of hard water into the        falcon tube. Add 51 ul of the sample into the same falcon tube        with hard water. Vortex to mix prior to dosing.

3. Dosing:

-   -   Vortex the sample prior to dosing.    -   Using a 25 ml serological pipette, pipette up and down to mix.        Pipette 15 ml of the mixture into each small Petri plate.    -   Let the mussels sit undisturbed for 24 hrs. Note the time and        date.

4. 24 hrs after treatment:

-   -   After 24 hrs after dosing, remove the treated water and check        for mussel mortality.    -   Dump out the treated water. Rinse with clean hard water 3 times        before adding water to each small Petri plate.    -   Repeat this process for all the Petri plates.    -   All the Petri dishes must be autoclaved after testing. After        being autoclaved, the jars will we washed with water.

5. Calculate the mortality

-   -   Mortality (%)=100*(Total dead mussels in the treatment-total        dead mussels in the blank)/Total mussels treatment        Studies with Commercial Compounds

Commercial compounds obtained from Sigma-Aldrich were examined at afinal concentration of 11.1 μg/ml. The results are shown in Table 1.

TABLE 1 Molluscicidal Effect of Commercial Compounds Conc No Structure[μg/ml] 24 hr 48 hr 72 hr 96 hr SAR-013

11.1 0 0 0 0 SAR-011

11.1 0 0 0 0 SAR-010

11.1 0 0 0 0 SAR-008

11.1 0 0 0 0 SAR-014

11.1 0 0 0 0 SAR-009

11.1 0 0 0 0 SAR-001

11.1 86.7 ± 5.8  96.7 ± 5.8  96.7 ± 5.8  96.7 ± 5.8  SAR-006

11.1 0 0 0 0 SAR-005

11.1 0 0 0 0 SAR-003

11.1 3.3 ± 5.7 10 ± 10 10 ± 10 10 ± 10 SAR-004

11.1 0 0 0 0 SAR-002

11.1 30 ± 10 66.7 ± 15.3 73.3 ± 11.5 76.7 ± 15.3

Synthetic Compounds

Synthesized compounds are screened against the quagga mussels at a finalconcentration of 11.1 μg/ml. The following procedure is used to obtainthe compounds.

Synthesis of amides: To the ice-cooled carboxylic acid (3 mmole)solution in dichloromethane (20 ml) is sequentially added1-ethyl-3-(3′-dimethylaminopropyl) carbodiimide (3.3 mmole) and4-dimethylaminopyridine (3 mmole). After 5 min, amine (3.3 mmole) isadded in the reaction solution. The reaction is slowly warmed to theroom temperature and lasted overnight. The reaction is extracted withethyl acetate (200 mL). The organic phase is dried with anhydrous sodiumsulfate. After evaporation under vacuum, the residue is run through asilica gel column with an appropriate ratio of ethyl acetate in hexane.The yield of the final products range from 85% to 90%. The finalproducts are characterized with proton NMR.

N-Cyclopentylcinnamamide (SAR-023): ¹H NMR (CDCl₃): δ (ppm) 7.62 (d,J=15.6 Hz, 1H), 7.50 (d, J=7.0 Hz, 2H), 7.35 (m, 3H), 6.37 (d, J=15.6,1H), 5.61 (d, J=5.0, Hz, 1H, NH), 4.35 (sextet, J=7.0, 1H), 2.06 (m,2H), 1.71 (m, 2H), 1.64 (m, 2H), 1.46 (m, 2H).

N-(trans-Cinnamoyl)pyrrolidine (SAR-024): ¹H NMR (CDCl₃): δ (ppm) 7.70(d, J=15.5 Hz, 1H), 7.53 (d, J=7.0 Hz, 2H), 7.36 (m, 3H), 6.74 (d,J=15.5, 1H), 3.63 (t, J=7.0, 2H), 3.60 (t, J=7.0, 2H), 2.01 (quintet,J=7.0, 2H), 1.91 (quintet, J=7.0, 2H).

N-(trans-Cinnamoyl)piperidine (SAR-025): ¹H NMR (CDCl₃): δ (ppm) 7.64(d, J=15.5 Hz, 1H), 7.52 (d, J=7.2 Hz, 2H), 7.36 (m, 3H), 6.90 (d,J=15.5, 1H), 3.67 (s, 2H), 3.59 (s, 2H), 1.68 (m, 2H), 1.62 (m, 4H).

N-(trans-Cinnamoyl)hexamethyleneimine (SAR-026): ¹H NMR (CDCl₃): δ (ppm)7.70 (d, J=15.4 Hz, 1H), 7.52 (d, J=7.6 Hz, 2H), 7.36 (m, 3H), 6.88 (d,J=15.4, 1H), 3.63 (t, J=6.0, 2H), 3.61 (t, J=6.0, 2H), 1.76 (m, 4H),1.59 (m, 4H).

N-Cyclopentyldecanamide (SAR-020): ¹H NMR (CDCl₃): δ (ppm) 5.35 (br,1H), 4.22 (sextet, J=7.00, 1H), 2.12 (t, J=7.20, 2H), 1.98 (m, 2H),1.59-1.67 (m, 6H), 1.26-1.36 (m, 14H), 0.88 (t, J=7.00, 3H).

N-(Decanoyl)pyrrolidine (SAR-007): ¹H NMR (CDCl₃): δ (ppm) 3.45 (t,J=6.80, 2H), 3.40 (t, J=6.80, 2H), 2.24 (t, J=7.20, 2H), 1.94 (quintet,J=6.80, 2H), 1.84 (quintet, J=6.80, 2H), 1.62 (quintet, J=7.20, 2H),1.25-1.30 (m, 12H), 0.87 (t, J=7.20, 3H).

N-(Decanoyl)piperidine (SAR-021): ¹H NMR (CDCl₃): δ (ppm) 3.55 (t,J=5.20, 2H), 3.39 (t, J=5.20, 2H), 2.31 (t, J=7.60, 2H), 1.58-1.65 (m,4H), 1.52-1.57 (m, 4H), 1.20-1.30 (m, 12H), 0.87 (t, J=7.20, 3H).

N-(Decanoyl)hexamethyleneimine (SAR-022): ¹H NMR (CDCl₃): δ (ppm) 3.52(t, J=6.00, 2H), 3.42 (t, J=6.00, 2H), 2.30 (t, J=7.80, 2H), 1.66-1.74(m, 4H), 1.60-1.66 (m, 2H), 1.50-1.6.0 (m, 4H), 1.20-1.30 (m, 12H), 0.87(t, J=7.20, 3H).

N-Cyclopentyldecenamide (SAR-027): ¹H NMR (CDCl₃): δ (ppm) 6.82 (dt,J1=15.20, J2=7.20, 1H), 5.71 (d, J=15.20, 1H), 5.33 (br, 1H), 4.27(sextet, J=7.00, 1H), 2.15 (m, 2H), 2.10 (m, 2H), 1.67 (m, 2H), 1.60 (m,2H), 1.40 (m, 4H), 1.28 (m, 8H), 0.88 (t, J=7.00, 3H).

N-(Decenoyl)pyrrolidine (SAR-030): ¹H NMR (CDCl₃): δ (ppm) 6.90 (dt,J1=15.20, J2=7.00, 1H), 6.07 (d, J=15.20, 1H), 3.52 (t, J=6.30, 2H),3.50 (t, J=6.30, 2H), 2.19 (m, 2H), 1.96 (quintet, J=7.00, 2H), 1.85(quintet, J=7.00, 2H), 1.44 (m, 2H), 1.28 (m, 8H), 0.88 (t, J=7.00, 3H).

N-(Decenoyl)piperidine (SAR-031): ¹H NMR (CDCl₃): δ (ppm) 6.82 (dt,J1=15.20, J2=7.00, 1H), 6.23 (d, J=15.20, 1H), 3.59 (t, J=6.30, 2H),3.47 (t, J=6.30, 2H), 2.17 (m, 2H), 1.64 (quintet, J=5.60, 2H), 1.56(quintet, J=5.60, 4H), 1.44 (quintet, J=7.00, 2H), 1.28 (m, 8H), 0.88(t, J=7.00, 3H).

N-(Decenoyl)hexamethyleneimine (SAR-032): ¹H NMR (CDCl₃): δ (ppm) 6.91(dt, J1=15.20, J2=7.00, 1H), 6.21 (d, J=15.20, 1H), 3.57 (t, J=6.00,2H), 3.49 (t, J=6.00, 2H), 2.17 (m, 2H), 1.73 (m, 4H), 1.56 (m, 4H),1.45 (m, 2H), 1.28 (m, 8H), 0.88 (t, J=7.00, 3H).

N-(Decenoyl)piperidine (SAR-033): ¹H NMR (CDCl₃): δ (ppm) 6.82 (dt,J1=15.20, J2=7.00, 1H), 6.23 (d, J=15.20, 1H), 3.59 (t, J=6.30, 2H),3.47 (t, J=6.30, 2H), 2.17 (m, 2H), 1.64 (quintet, J=5.60, 2H), 1.56(quintet, J=5.60, 4H), 1.44 (quintet, J=7.00, 2H), 1.28 (m, 8H), 0.88(t, J=7.00, 3H).

The results are shown in Table 2.

TABLE 2 Potency of synthesized amides toward quagga mussels Conc NoStructure [μg/ml] 24 hr 48 hr 72 hr 96 hr SAR-020

11.1 75 ± 7  75 ± 7  75 ± 7  75 ± 7  SAR-007

11.1 35 ± 7  50 ± 14 55 ± 21 65 ± 21 SAR-021

11.1 55 ± 21 55 ± 21 60 ± 14 65 ± 7 SAR-022

11.1 35 ± 7  40 ± 14 40 ± 14 45 ± 21 SAR-023

11.1 0 0 0 0 SAR-024

11.1 0 0 0 0 SAR-025

11.1 0 0 0 0 SAR-026

11.1 0 0 0 0 SAR-027

11.1 85 ± 7  95 ± 7  95 ± 7  95± 7  SAR-031

111 20 ± 14 35 ± 35 35± 35 40± 28 SAR-032

11.1 45 ± 21 50 ± 14 80 ± 14 80 ± 14 SAR-033

11.1 70 ± 14 75 ± 21 75 ± 21 75 ± 21

Example 2 Erwinia Extracts

Erwinia carotovora is grown on LB broth (per liter: 10 g tryptone, 5 gyeast extract, 10 g NaCl, pH=7.5). Inoculum is grown by streaking a TSA(tryptic soy agar) plate from a glycerol stock. Purity of the culture isconfirmed through visual inspection of colony morphology. Using asterile 10 μL loop, colonies are collected from the agar surface andresuspended in 50 ml of LB broth in a 250 ml non-baffled Erlenmeyerflask with screw cap. The liquid culture is incubated for 48-72 hours at200 rpm and 25° C.

After 72 hr, the whole broth is extracted with ethyl acetate. Theorganic phase is dried under vacuum. The dried extracted is made a 5.0mg/mL solution in dimethyl sulfoxide (DMSO). Then, such solution (100μL) is added into 45 mL hard water. The final concentration of ethylacetate extracts is 11.1 ppm.

Data shown in Table 3 indicates that bioactive compounds against thequagga mussels are produced in Erwinia carotovora when grown in the LBmedia. The compound 37 (FIG. 1 b) described above is one of the lactonesproduced by E. carotovora grown in the LB media [Gu″nter Brader, SolveigSjo″blom, Heidi Hyytia″inen, Karen Sims-Huopaniemi, and E. Tapio Palva,Altering Substrate Chain Length Specificity of an AcylhomoserineLactone. Synthase in Bacterial Communication, The Journal of BiologicalChemistry, 2005, 280(11) 10403-10409].

TABLE 3 Efficacy of ethyl acetate extracts of Erwinia carotovora grownin the LB broth % % % % % % mortality mortality mortality mortalitymortality mortality Treatments (24 hr) (48 hr) (72 hr) (96 hr) (120 hr)(144 hr) Erwinia 30 ± 0 75 ± 7 80 ± 0 80 ± 0 80 ± 0 90 ± 14 carotovoraBlank 0 0 0 0 0 0

Example 3 Isolation of Molluscicidal Compounds from Pseudomonas Study AFractionation of Compounds

The following procedure is used for the fractionation of compoundsextracted from washed cells of Pseudomonas fluorescens CL-145A:

The cell pellet derived from the 10-L fermentation P. fluorescens CL145A (ATCC 55799) in FM2 growth medium is suspended in dilution bufferand extracted with Amberlite XAD-7 resin (Asolkar, R. N., Jensen, P. R.,Kauffman, C. A., Fenical, W. 2006. Daryamides A-C, Weakly CytotoxicPolyketides from a Marine-Derived Actinomycete of the Genus Streptomycesstrain CNQ-085 J. Nat. Prod. 69:1756-1759; Williams, P. G., Miller, E.D., Asolkar, R. N., Jensen, P. R., Fenical, W. 2007. Arenicolides A-C,26-Membered Ring Macrolides from the Marine Actinomycete Salinisporaarenicola. J. Org. Chem. 72:5025-5034) by shaking the cell suspensionwith resin at 225 rpm for two hours at room temperature. The resin andcell mass are collected by filtration through cheesecloth and washedwith DI water to remove salts. The resin, cell mass, and cheesecloth arethen soaked for 2 h in acetone after which the acetone is filtered anddried under vacuum using rotary evaporator to give the crude extract.The crude extract is then fractionated by using reversed-phase C18vacuum liquid chromatography (H₂O/CH₃OH; gradient 90:20 to 0:100%) togive 7 fractions. These fractions are then concentrated to dryness usingrotary evaporator and the resulting dry residues are screened forbiological activity using both a live mussel jar-test bioassay withquagga mussels as well as a cell-based assay with a freshwater snailembryo cell line (Biomphalaria glabrata). The bioassays are described inmore detail in examples #2 and #3. The active fractions are thensubjected to reversed/normal phase HPLC (Spectra System P4000 (ThermoScientific) to give pure compounds, which are then screened in abovementioned bioassays to locate/identify the active compounds. To confirmthe identity of the compound, additional spectroscopic data such asLC/MS and NMR is recorded.

A diagram of the method used is shown in FIG. 3. Based on both livemussel and snail cell assay, fractions #4 and #5 contain activecompounds. Of all compounds separated by HPLC (C-18 column,water:acetonitrile gradient solvent system (0-10 min; 30-40% aqueousCH₃CN, 10-20 min; 40-60% aqueous CH₃CN, 20-60 min; 60-80% aqueous CH₃CN,60-65 min; 80-100% aqueous CH₃CN) at 2.5 mL/min flow rate and UVdetection of 210 nm, peaks number 20, retention time 51.66 min, 21,retention time 52.56 min, and 22 A retention time 59.61 min inhibits thegrowth (e.g. low OD600 value) of snail cells in the bioassay.

Mass spectroscopy analysis of active peaks is performed on a ThermoFinnigan LCQ Deca XP Plus electrospray (ESI) instrument using bothpositive and negative ionization modes in a full scan mode (m/z 100-1500Da) on a LCQ DECA XP^(plus) Mass Spectrometer (Thermo Electron Corp.,San Jose, Calif.). Thermo high performance liquid chromatography (HPLC)instrument equipped with Finnigan Surveyor PDA plus detector,autosampler plus, MS pump and a 4.6 mm×100 mm Luna C18 5 μm column(Phenomenex). The solvent system consists of water (solvent A) andacetonitrile (solvent B). The mobile phase begins at 10% solvent B andis linearly increased to 100% solvent B over 20 min and then kept for 4min, and finally returned to 10% solvent B over 3 min and kept for 3min. The flow rate is 0.5 mL/min. The injection volume was 10 μL and thesamples are kept at room temperature in an auto sampler. The compoundsare analyzed by LC-MS utilizing the LC and reversed phasechromatography. Mass spectroscopy analysis of the present compounds isperformed under the following conditions: The flow rate of the nitrogengas was fixed at 30 and 15 arb for the sheath and aux/sweep gas flowrate, respectively. Electrospray ionization was performed with a sprayvoltage set at 5000 V and a capillary voltage at 35.0 V. The capillarytemperature was set at 400° C. The data was analyzed on Xcalibursoftware. The active compound in peak #20 has a molecular mass of1294.75 in positive ionization mode. The LC-MS chromatogram for anotheractive compound (peak #22A) suggests a molecular mass of 1320.83 inpositive ionization mode.

For structure elucidation, the partially purified compound from activepeak #20 is further analyzed using a 600 MHz NMR instrument, and has δvalues at δ 9.25, 8.36, 8.06, 7.82, 7.71, 7.52, 7.45, 6.82, 6.36, 6.08,5.42, 5.39, 5.30, 5.14, 4.68, 4.42, 4.31, 4.16, 4.11, 4.07, 3.95-3.86,3.83, 3.72, 3.66, 3.53, 3.48, 3.37, 3.17, 3.06, 2.56, 2.53, 2.45, 2.32,2.21, 2.02, 1.96, 1.84, 1.72, 1.65, 1.61, 1.51, 1.48-1.37, 1.32, 1.12,0.94, 0.91, 0.68 in CDCl₃. The NMR data indicates that the compoundcontains amino, ester, carboxylic acid, phenyl, indole, aliphaticmethyl, ethyl, methylene, oxymethylene, methine, o-methyl, oxymethineand sulfur groups.

Similarly, HPLC analysis on a C-18 column and acetonitrile: watersolvent system (0-10 min; 35-45% aqueous CH₃CN, 10-20 min; 45-60%aqueous CH₃CN, 20-50 min; 60-85% aqueous CH₃CN, 50-60 min; 85-100%aqueous CH₃CN, 60-70 min; 100% CH₃CN) at 10 mL/min flow rate and UVdetection of 210 nm of the active fraction #4 using bioassay guidedfractionation yielded multiple peaks with activity against both livemussels and snail embryo cells. Most of the activity is concentrated inpeaks #27 retention time 47.73 min and #30 retention time 51.52 min.

Peaks #27 and #30 are further analyzed by LC/MS. Based on the results,peak # 27 contains multiple compounds with the two main componentshaving a mass of roughly 643 and 984. Peak #30 contains fewer compounds,and the mass analysis suggests a molecular mass around 546 for the maincomponent under the peak.

Mussel Bioassay Test

This live mussel bioassay test is used to guide the identification ofactive compounds through sample fractionation using HPLC and LC-MS asanalytical tools.

Twenty freshly collected quagga mussels is placed in a jar containing250 mL of de-chlorinated tap water at room temperature. Jars are kept atroom temperature and connected into a manifold providing constant airsupply through bubbling. Each test subject (HPLC fraction or peak)dissolved in DMSO is pipetted into jars separately at a concentration of1-5 mg, and the mussels are incubated with the test subject for 24hours. After the incubation period, water in each jar is discarded, andthe mussels are rinsed with fresh water and transferred into open glasspetri dishes for a 10-day observation period. Mussels are checked dailyfor mortality, and the dead mussels are removed and discarded. Eachtreatment is carried out in three replicates, and in the end of the10-day incubation period, % mortality is calculated for each treatment.

Cell-Based Assay

As an alternative method, this cell-based assay is used as a tool tofacilitate the isolation and identification of active compounds in theP. fluorescens cells after fermentation. Embryonic cells of a freshwatersnail (Biomphalaria glabrata, ATCC CRL-1494) are used as a model systemfor mussel digestive gland epithelial cells known to be susceptible forthe P. fluorescens biotoxins. For the assay, 200 uL of actively growingcells in a complete growth medium containing Drosophila medium, fetalcalf serum, d-galactose, and lactalbumin is added into each well of asterile 96-well plate. The test compound (HPLC fraction or peak at 20mg/mL) dissolved in DMSO is added into each well, and the plate iscovered and incubated in a controlled environment at 23° C. and 5% CO₂.Activity (growth inhibition=low turbidity) is measured at 600 nm using aSpectraMax plate reader with the SoftMax Pro software, and compared tothe negative control with pure DMSO as a test compound. Each treatmentis run in four replicates, and one replicated positive control treatmentis included in each plate.

Study B Methods and Materials

The following procedure is used for the purification of compoundsextracted from cell culture of Pseudomonas fluorescens and is summarizedin FIG. 3. Specifically, the cell pellet derived from the 10-Lfermentation P. fluorescens CL 145A (ATCC 55799) in FM2 growth medium issuspended in dilution buffer and extracted with Amberlite XAD-7 resin(Asolkar, R. N., Jensen, P. R., Kauffman, C. A., Fenical, W. 2006.Daryamides A-C, Weakly Cytotoxic Polyketides from a Marine-DerivedActinomycete of the Genus Streptomyces strain CNQ-085 J. Nat. Prod.69:1756-1759 and Williams, P. G., Miller, E. D., Asolkar, R. N., Jensen,P. R., Fenical, W. 2007. Arenicolides A-C, 26-Membered Ring Macrolidesfrom the Marine Actinomycete Salinispora arenicola. J. Org. Chem.72:5025-5034) by shaking the cell suspension with resin at 225 rpm fortwo hours at room temperature. The resin and cell mass are collected byfiltration through cheesecloth and washed with DI water to remove salts.The resin, cell mass, and cheesecloth are then soaked for 2 h in acetoneafter which the acetone is filtered and dried under vacuum using rotaryevaporator to give the crude extract. The crude extract is thenfractionated by using reversed-phase C18 vacuum liquid chromatography(H₂O/CH₃OH; gradient 90:20 to 0:100%) to give 7 fractions. Thesefractions are then concentrated to dryness using rotary evaporator andthe resulting dry residues are screened for biological activity usingboth a live mussel jar-test bioassay with quagga mussels as well as acell-based assay with a freshwater snail embryo cell line (Biomphalariaglabrata). The active fractions are then subjected to reversed phaseHPLC (Spectra System P4000 (Thermo Scientific) to give pure compounds,which are then screened in above mentioned bioassays to locate/identifythe active compounds. To confirm the identity of the compound,additional spectroscopic data such as LC/MS and NMR is recorded.

The active fraction 4 is further subfractionated by using Sephadex LH 20size exclusion chromatography to give 7 sub fractions. Purification ofPilferolide A and 11-Hydroxy-12-ene-Octadecanoic Acid is performed byusing HPLC C-18 column (Phenomenex, Luna 10u C18(2) 100 A, 250×30),water:acetonitrile gradient solvent system (0-10 min; 50-60% aqueousCH₃CN, 10-20 min; 60-75% aqueous CH₃CN, 20-45 min; 75-100% aqueousCH₃CN, 45-55 min; 100% CH₃CN, 55-70 min; 100-50% aqueous CH₃CN) at 8mL/min flow rate and UV detection of 210 nm, the active peaks number 21,retention time 45.59 min, and 23, retention time 48.53 min.

Mass spectroscopy analysis of active peaks is performed on a ThermoFinnigan LCQ Deca XP Plus electrospray (ESI) instrument using bothpositive and negative ionization modes in a full scan mode (m/z 100-1500Da) on a LCQ DECA XP^(plus) Mass Spectrometer (Thermo Electron Corp.,San Jose, Calif.). Thermo high performance liquid chromatography (HPLC)instrument equipped with Finnigan Surveyor PDA plus detector,autosampler plus, MS pump and a 4.6 mm×100 mm Luna C18 5 μm column(Phenomenex). The solvent system consisted of water (solvent A) andacetonitrile (solvent B). The mobile phase begins at 10% solvent B andis linearly increased to 100% solvent B over 20 min and then kept for 4min, and finally returned to 10% solvent B over 3 min and kept for 3min. The flow rate is 0.5 mL/min. The injection volume was 10 μL and thesamples are kept at room temperature in an auto sampler. The compoundsare analyzed by LC-MS utilizing the LC and reversed phasechromatography. Mass spectroscopy analysis of the present compounds isperformed under the following conditions: The flow rate of the nitrogengas was fixed at 30 and 15 arb for the sheath and aux/sweep gas flowrate, respectively. Electrospray ionization was performed with a sprayvoltage set at 5000 V and a capillary voltage at 35.0 V. The capillarytemperature was set at 400° C. The data was analyzed on Xcalibursoftware. The active compound Piliferolide A has a molecular mass of295.65 in negative ionization mode. The LC-MS chromatogram for anotheractive compound suggests a molecular mass of 297.74 in negativeionization mode.

For structure elucidation, the purified compound Piliferolide A with amolecular weight 296 is further analyzed using a 500 MHz NMR instrument;the reference is set on the internal standard tetramethylsilane (TMS,0.00 ppm). The compound has ¹H NMR δ values at 5.62, 5.42, 4.55, 3.97,2.58, 2.35, 2.04, 1.88, 1.73, 1.64, 1.54, 1.39, 0.92 and has ¹³C NMRvalues of δ 179.1, 133.3, 131.3, 81.9, 72.6, 37.3, 35.4, 32.1, 31.3,29.5, 29.4, 29.0, 28.6, 27.8, 25.4, 25.3, 22.5, 13.3. The detailed 1Dand 2D NMR analysis confirm the structure for the compound asPiliferolide A as a known compound.

The second purified compound with a molecular weight 298 is furtheranalyzed using a 500 MHz NMR instrument, and has ¹H NMR δ values at5.61, 5.41, 3.96, 2.27, 2.04, 1.69, 1.51, 1.42, 1.32, 0.92 and ¹³C NMRvalues of δ 176.6, 133.2, 132.6, 73.5, 37.5, 33.9, 32.4, 31.6, 29.8,29.7, 29.6, 29.4, 29.3, 29.1, 25.7, 24.9, 22.8, 14.3. The detailed 1Dand 2D NMR analysis confirm the structure to the compound which is notreported for microbial source; Molecular formula C₁₈H₃₄O₃. The structureof the compound, 11-Hydroxy-12-ene-Octadecanoic Acid is shown below:

The potency of compounds isolated from Pseudomonas cell culture istested using procedures described above. The results are shown below inTable 4.

TABLE 4 Molluscicidal Effects of Piliferolide A and11-Hydroxy-12-ene-octadecanoic acid Conc % mortality % mortality %mortality % mortality Structure [μg/ml] 24 hr 48 hr 72 hr 96 hr

16 53.3 ± 15.3 53.3 ± 15.3 70 ± 10 80 ± 10

16 0 20 ± 20 33.3 ± 20.8  40 ± 26.5

Example 5 Kaolin Effects

The effect of kaolin clay on the efficacy of a microbial biopesticidebased on P. fluorescens bacteria is tested in a biobox study conductedat 11.8° C. On the first day the experiment, kaolin clay is applied tothe biobox from a concentrated stock solution via a peristaltic pump sothat the final turbidity in the biobox is approximately 20 NTU(normalized turbidity units). Fifty quagga mussels are placed in 1-footlong acrylic tubes closed with a nylon mesh at both ends, and the tubesare placed in the bottom of the biobox for the treatment. The durationof the clay application is 6 hours, after which the mussels in theacrylic tubes were exposed to fresh running water in the biobox for 18hours. The following day, extra clay is cleaned off from bottom thebiobox, and the biopesticide in aqueous suspension was applied via aperistaltic pump to a final concentration of 200 ppm. After the 6-hourbiopesticide treatment, mussels in tubes are incubated in the bioboxwith fresh running water at a rate of 1 gallon per minute. Mussels areobserved and counted weekly for 5 weeks for determination of %mortality. The control treatments included an untreated control, atreatment with only kaolin clay (with no biopesticide) and a treatmentwith only biopesticide (with no clay pre-treatment). All treatments arerun in three replicates.

Results presented in Table 5 and FIG. 4 show a significant increase inmortality for mussels exposed to kaolin clay 18 hours before thebiopesticide treatment compared with mussels with no clay pre-treatment.This phenomenon can be explained by increased siphoning activity ofmussels harvested and treated in cold (11.8° C.) water during the periodof low biological activity. This increased siphoning results in greateruptake of pesticide product, which in turn results in increased musselmortality.

TABLE 5 Efficacy of biopesticide expressed as % mortality measured ateach time point (days) % mortality 1 9 16 21 27 34 Untreated control 0 00 0 0 0 Kaolin 20 NTU 0 0 0 0 0 1 Kaolin 20 NTU + 200 ppm 0 35 64 71 7783 200 ppm 0 22 46 55 58 63

Example 6 Effects of Gamma-Dodecalactone and N-Decenoyl)Pyrrolidine onSnails

Snail experiments: An appropriate amount of a testing compound isdissolved in acetone (2 mL) first. The solution was added into 2.5 gramof corn starch and mixed well. The resulting mixture is transferred to aPetri dish (Φ 25 mm). The Petri dish is then put in the hood for naturaldry. After drying, water (2 mL) is added into the Petri dish to makepaste.

Brown garden snails (Cantareus aspersus) are collected from a housegarden and raised at least 1 day in lab with cabbage or red carrot. Fiveindividuals with a similar size are chosen for each treatment andtransferred into a 1 L beaker. To make the snail active, some water issprayed on them and in the beaker by using hand-sprayer. After sprayingwater, the Petri dish with chemical-containing corn starch is placedinto the beaker the beaker is covered on the top with aluminum foil.Eating behavior, consumed amount of corn starch and mortality at 24 hris recorded.

The data indicates (set forth in Table 6) that gamma-dodecalactone(SAR-014) at 100 mg/gram corn starch would strongly repel brown gardensnails. However, N-decenoyl)pyrrolidine (SAR-030) in 100 mg/gram cornstarch would kill all brown garden snails after they ate.

TABLE 6 Chemical effects on brown garden snail Consumed Dose (mg/gramEating amount of treatment chemical corn starch) behavior corn starch 24hr mortality control 0 All Finishing all 0% individuals corn starch atecorn starch within 2 hr 1 SAR-014 100 All 0% after 0% individuals 24 hrquickly escaped from the starch 2 SAR-030 100 Four Less than Allindividuals 5% of corn individuals out of five ate starched which atethe a little bit of were corn starch starch and consumed were deadwalked away. after 24 hrAlthough this invention has been described with reference to specificembodiments, the details thereof are not to be construed as limiting, asit is obvious that one can use various equivalents, changes andmodifications and still be within the scope of the present invention.

Various references are cited throughout this specification, each ofwhich is incorporated herein by reference in its entirety.

1. An isolated compound having the following characteristics (a) isobtainable from a microorganism; (b) is toxic to a member of aGastropoda and/or Bivalvia class of molluscs and (c) has a molecularweight selected from the group consisting of: about 540-550, and about1280-1335 as determined by Liquid Chromatography/Mass Spectroscopy(LC/MS).
 2. The compound according to claim 1, wherein said compound istoxic to at least one of mussels, snails and slugs.
 3. The compositionaccording to claim 1, wherein said compound has (a) a molecular weightof about 1280-1310 as determined by Liquid Chromatography/MassSpectroscopy (LC/MS); (b) has ¹H NMR values of δ 9.25, 8.36, 8.06, 7.82,7.71, 7.52, 7.45, 6.82, 6.36, 6.08, 5.42, 5.39, 5.30, 5.14, 4.68, 4.42,4.31, 4.16, 4.11, 4.07, 3.95-3.86, 3.83, 3.72, 3.66, 3.53, 3.48, 3.37,3.17, 3.06, 2.56, 2.53, 2.45, 2.32, 2.21, 2.02, 1.96, 1.84, 1.72, 1.65,1.61, 1.51, 1.48-1.37, 1.32, 1.12, 0.94, 0.91, 0.68 and (c) has an (HighPressure Liquid Chromatography) (HPLC) retention time of about 50-55 minon a reversed phase C-18 HPLC column using a water:acetonitrile gradientsolvent system (0-10 min; 30-40% aqueous CH₃CN, 10-20 min; 40-60%aqueous CH₃CN, 20-60 min; 60-80% aqueous CH₃CN, 60-65 min; 80-100%aqueous CH₃CN) at 2.5 mL/min flow rate and UV detection of 210 nm. 4.The compound according to claim 3, wherein said compound has a molecularweight of about
 1295. 5. The compound according to claim 1, wherein saidcompound (a) has a molecular weight of about 1310-1335 as determined byLC/MS; (b) has an HPLC retention time of about 55-60 min on a reversedphase C-18 HPLC column using a water:acetonitrile gradient solventsystem (0-10 min; 30-40% aqueous CH₃CN, 10-20 min; 40-60% aqueous CH₃CN,20-60 min; 60-80% aqueous CH₃CN, 60-65 min; 80-100% aqueous CH₃CN) at2.5 mL/min flow rate and UV detection of 210 nm.
 6. The compoundaccording to claim 5, wherein said compound has a molecular weight ofabout
 1321. 7. The compound according to claim 1, wherein said compoundhas a molecular weight of about 540-550 as determined by LC/MS; (d) hasan HPLC retention time of about 50-55 min on a reversed phase C-18 HPLCcolumn using a water:acetonitrile solvent system (0-10 min; 35-45%aqueous CH₃CN, 10-20 min; 45-60% aqueous CH₃CN, 20-50 min; 60-85%aqueous CH₃CN, 50-60 min; 85-100% aqueous CH₃CN, 60-70 min; 100% CH₃CN)at 10 mL/min flow rate and UV detection of 210 nm.
 8. The compoundaccording to claim 7, wherein said compound has a molecular weight ofabout
 546. 9. A composition comprising a water:acetonitrile solventsystem (0-10 min; 35-45% aqueous CH₃CN, 10-20 min; 45-60% aqueous CH₃CN,20-50 min; 60-85% aqueous CH₃CN, 50-60 min; 85-100% aqueous CH₃CN, 60-70min; 100% CH₃CN) at 10 mL/min flow rate and UV detection of 210 nmfraction obtainable from a Pseudomonas species cell suspension by HPLCwith a retention time of about 45-50 min, said fraction comprising atleast two compounds that (a) are toxic to a member of a Gastropodaand/or Bivalvia class; (b) have molecular weights between about 630-660and between about 970-1000 as determined by LC/MS.
 10. The compositionaccording to claim 9, wherein said compounds have molecular weights ofabout 643 and about
 984. 11. A composition comprising at least one ormore substances effective for controlling a member of a Gastropoda andBivalvia class and an inert material.
 12. The composition according toclaim 11, wherein said substances are derived from a Pseudomonas speciesor cell suspension derived from a Pseudomonas species.
 13. Thecomposition according to claim 11, wherein said substances are derivedfrom Pseudomonas fluorescens or cell suspension derived from Pseudomonasfluorescens.
 14. The composition according to claim 11, wherein saidsubstances are derived from a Pseudomonas strain, having the identifyingcharacteristics of Pseudomonas ATCC
 55799. 15. The composition accordingto claim 11, wherein the composition comprises a substance that is acell suspension comprising cells having the toxin producingcharacteristics of Pseudomonas ATCC
 55799. 16. The composition accordingto claim 11, wherein the substances are one or more toxins derived froma Pseudomonas species.
 17. The composition according to claim 11,wherein the substances are one or more toxins derived from an organismhaving the identifying characteristics of Pseudomonas ATCC
 55799. 18.The composition according to claim 11, wherein said substance effectivefor controlling Dreissana and/or Biomphalaria species is a compoundhaving the following characteristics (a) is obtainable from aPseudomonas species; (b) is toxic to a member of a Gastropoda andBivalvia class and (c) has a molecular weight selected from the groupconsisting of: about 540-550, and about 1280-1335 as determined byLiquid Chromatography/Mass Spectroscopy (LC/MS).
 19. A method forcontrolling one or more molluscs in a location where control is desiredcomprising introducing into said location at least one of (a) a cellsuspension or extract derived from Erwinia sp. Cells; (b) one or morecompounds, wherein said compounds are lactone, lactam, carbamate,carboxylic acid and/or amide compounds or composition comprising saidcompounds, with the proviso that said compounds are notgamma-octalactone, gamma-nonalactone, gamma-decanolactone,gamma-undecalactone, N-cyclpentylcinnamamide,N-(trans-cinnamoyl)pyrrolidine, N-(trans-Cinnamoyl)piperidine andN-(trans-Cinnamoyl)hexamethyleneimine, 4-hydroxydodecanoic acid anddodecanoic acid and with the proviso that the composition is not aPseudomonas culture, extract or suspension; (c) one or more compounds ofclaim 1; (d) a composition comprising a water:acetonitrile solventsystem (0-10 min; 35-45% aqueous CH₃CN, 10-20 min; 45-60% aqueous CH₃CN,20-50 min; 60-85% aqueous CH₃CN, 50-60 min; 85-100% aqueous CH₃CN, 60-70min; 100% CH₃CN) at 10 mL/min flow rate and UV detection of 210 nmfraction obtainable from a Pseudomonas species cell suspension by HPLCwith a retention time of about 45-50 min, said fraction comprising atleast two compounds that (i) are toxic to a member of a Gastropoda andBivalvia class; (ii) have molecular weights between about 630-660 andbetween about 970-1000 as determined by LC/MS, in amounts effective tocontrol said molluscs.
 20. The method according to claim 19, whereinsaid molluscs species are controlled by inducing death in said molluscsspecies.
 21. The method according to claim 19, wherein said compoundsintroduced into said location, are lactone, lactam, carbamate,carboxylic acid and/or amide and said compounds are members of a familyof compounds selected from the group consisting of: (a) family I,wherein a family I compound possesses following chemical structure:

Wherein X is carbon; Y is oxygen; A and M are carbon, oxygen, nitrogen,sulfur and n is 1 to 21 Wherein (R)z represents number Z of the numberof substituents on the group R on the ring wherein R and thesubstituents on R are selected from the group consisting of hydrogen,hydroxyl, alkyl hydroxyl, alkenyl hydroxyl, alkynyl hydroxyl, alkyloxy,alkenyloxyl, alkynylxoy, cycloalkyl, cycloalkenyl, alkyl, alkenyl,alkynyl, heterocyclyl, heteroaryl, aromatic, aryl group, NH-substituted,and N,N-substituted group; the length of the R chain is from 1 to 25atoms, and Z is 0, 1, 2, 3; (b) family II, wherein a family II compoundpossesses following chemical structure:

Wherein X is carbon; Y is oxygen; A, B and M are carbon, oxygen,nitrogen and sulfur; Wherein (R)z represents number Z of the number ofsubstituents on the group R on the ring; R and the substituents on R isselected from the group consisting of a hydrogen, hydroxyl, alkylhydroxyl, alkenyl hydroxyl, alkynyl hydroxyl, alkyloxy, alkenyloxyl,alkynylxoy, alkyl, alkenyl, alkynyl, heterocyclyl, aromatic, aryl group,NH-substituted, and N,N-substituted group; the length of the R chain isfrom 1 to 25 atoms, and Z is 0, 1, 2, 3; (c) family III, wherein afamily III compound possesses following chemical structure:

Wherein X is carbon, Y is oxygen; Z is hydrogen, hydroxyl, alkenylhydroxyl, alkynyl hydroxyl, alkyl, alkenyl, alkynyl, heterocyclyl,aromatic, aryl group, NH-substituted, or N,N-substituted group. WhereinR is alkenyl hydroxyl, alkynyl hydroxyl, alkyl, alkenyl, alkynyl,heterocyclyl, aromatic, aryl group, NH-substituted, or N,N-substitutedgroup 1 to 50 atoms in length.
 22. The method according to claim 21,wherein R in family I, II and III compounds are from 7 to 17 atoms inlength.
 23. The method according to claim 21, wherein said compound hasthe structure

wherein Y and M are oxygen, A and X are carbon and n is 2 or 3, R is aC7 or C8 alkyl and z is 0, wherein when n is 2 and R is a C7 alkyl, R isattached to A.
 24. The method according to claim 21, wherein saidcompound is a sarmentine analog having the following structure:

Wherein R₁ is an alkyl, alkenyl, alkynyl, heterocyclyl, aromatic, arylgroup, NH-substituted, or N,N-substituted group, wherein the length ofR₁ chain is from 4 to 20 atoms, Wherein R₂ and R₃ are alkyl, alkenyl,alkynyl, cycloalkyl, cycloalkenyl, aromatic, arylalkyl, heterocyclyl orheteroaryl; or alternatively R₂+R₃+N can be an N-containing heterocyclicmoiety, Wherein when R₂+R₃+N is an N-containing heterocyclic moiety, R1is an alkyl, alkenyl, alkynyl, heterocyclyl, NH-substituted, orN,N-substituted group.
 25. The method according to claim 24, wherein thelength of R₁ chain is from 6 to 12 atoms.
 26. The method according toclaim 19, wherein said compound is a lactone and has a hydroxylatedunsaturated fatty acid lactone structure comprising at least one lactonemoiety which is a 5 membered γ-lactone, at least one unsaturated moietyand at least one alcohol group; a molecular weight from 285 to about 310in the core structure; at least 15 carbons and at least 3 oxygens. 27.The method according to claim 26, wherein said compound has thestructure

wherein: X are each independently —O, —NR₁, or —S, wherein R₁ is —H orC₁-C₆alkyl; n=0 to 15, R₂ to R₄ are each independently —H, alkyl,substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substitutedalkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, substituted heterocyclic, cycloalkyl, substitutedcycloalkyl, alkoxy, substituted alkoxy, thioalkyl, substitutedthioalkyl, hydroxy, halogen, amino, amido, carboxyl, —C(O)H, acyl,oxyacyl, carbamate, sulfonyl, sulfonamide, or sulfuryl; m=double bond ortriple bond.
 28. The method according to claim 19, wherein said compoundis has a hydroxylated unsaturated fatty acid structure comprising atleast one carboxylic acid moiety, at least one unsaturated moiety and atleast one alcohol group; a molecular weight from 285 to about 310 in thecore structure; at least 15 carbons and at least 3 oxygens.
 29. Themethod according to claim 28, wherein said compound has the structure

wherein: X are each independently —OH, —NR₁, or —S, wherein R₁ is —H orC₁-C₆ alkyl; n=0 to 15, R₂ to R₄ are each independently —H, alkyl,substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substitutedalkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl,heterocyclic, substituted heterocyclic, cycloalkyl, substitutedcycloalkyl, alkoxy, substituted alkoxy, thioalkyl, substitutedthioalkyl, hydroxy, halogen, amino, amido, carboxyl, —C(O)H, acyl,oxyacyl, carbamate, sulfonyl, sulfonamide, or sulfuryl; m=double bond,triple bond.
 30. The method according to claim 19, wherein the compoundis selected from the group consisting of: (a) a compound set forth inFIG. 1; (b) a lactone selected from the group consisting ofgamma-dodecalactone, delta-tridecalactone, piliferolide A andalpha-heptyl-gamma-butyrolactone and (c) a sarmentine analog selectedfrom the group consisting of N-Cyclopentyldecanamide,N-(Decanoyl)pyrrolidine, N-(Decanoyl)piperidine,N-(Decanoyl)hexamethyleneimine, N-Cyclopentyldecenamide,(N-(Decenoyl)pyrrolidine, N-(Decenoyl)piperidine,N-(Decenoyl)hexamethyleneimine and N-(Decenoyl)piperidine and (d)11-hydroxy-12-ene-octadecanoic acid.
 31. A method for controlling one ormore molluscs comprising introducing a substance and one or more inertmaterials in a location where control is desired in amounts effectivefor controlling said molluscs.
 32. The method according to claim 31,wherein said substance for controlling molluscs is present in an amountto result in at least about a 20% mortality of said molluscs relative tountreated control and said inert material is present in an amountsufficient to increase mortality rate of said substance for controllingmolluscs at least about 20%.
 33. The method according to claim 31,wherein said location is a liquid wherein said liquid is a body of wateror paint.
 34. The method according to claim 31, wherein said location isa solid surface selected from the group consisting of plastic, concrete,wood, fiberglass, pipes made of iron and polyvinyl chloride, surfacescovered with coating materials and/or paints.
 35. A method forincreasing the efficacy of one or more substances for controllingmolluscs comprising introducing in a location where control is desiredone or more inert materials in amounts effective to increase efficacy ofsaid substance when introduced in said location.
 36. The methodaccording to claim 35, wherein said inert materials increases theefficacy of said substances at least about 20%.
 37. The method accordingto claim 35, wherein said inert materials are derived from a claymineral.
 38. The method according to claim 35, wherein said inertmaterials are kaolinite, smectite, attapulgite or a combination of theforegoing.
 39. A composition for controlling one or more molluscs in alocation where control is desired and/or inducing death in one or moremolluscs comprising one or more lactones, lactams, carbamates,carboxylic acids and/or amides, again with the proviso that saidcompound is not gamma-octalactone, gamma-nonalactone,gamma-decanolactone, gamma-undecalactone, N-cyclpentylcinnamamide,N-(trans-cinnamoyl)pyrrolidine, N-(trans-Cinnamoyl)piperidine andN-(trans-Cinnamoyl)hexamethyleneimine, 4-hydroxydecanoic acid anddecanoic acid and with the proviso that the composition is not aPseudomonas culture, extract or suspension.
 40. A method for controllingone or more molluscs comprising the steps of: (a) preparing a cellsuspension or extract derived from Erwinia sp. cells; and (b)introducing said suspension or extract into a location where control isdesired in an amount effective to control said molluscs.
 41. Anantifouling paint comprising an antivegetative, biocidal effectiveamount of the composition of claim 11 in a paint carrier.